Pesticidal compositions

ABSTRACT

The invention disclosed in this document is related to the field of pesticides and their use in controlling pests. A compound having the following structure is disclosed.

CROSS-REFERENCE TO RELATED APPLICATION

This application claims the benefit of U.S. Provisional Application Ser.No. 61/065,475 filed on Feb. 12, 2008 the entire contents of such ishereby incorporated by reference.

FIELD OF THE INVENTION

The invention disclosed in this document is related to the field ofpesticides and their use in controlling pests.

BACKGROUND OF THE INVENTION

Pests cause millions of human deaths around the world each year.Furthermore, there are more than ten thousand species of pests thatcause losses in agriculture. These agricultural losses amount tobillions of U.S. dollars each year. Termites cause damage to variousstructures such as homes. These termite damage losses amount to billionsof U.S. dollars each year. As a final note, many stored food pests eatand adulterate stored food. These stored food losses amount to billionsof U.S. dollars each year, but more importantly, deprive people ofneeded food.

There is an acute need for new pesticides. Insects are developingresistance to pesticides in current use. Hundreds of insect species areresistant to one or more pesticides. The development of resistance tosome of the older pesticides, such as DDT, the carbamates, and theorganophosphates, is well known. But, resistance has even developed tosome of the newer pesticides. Therefore, a need exists for newpesticides and particularly for pesticides that have new modes ofaction.

The examples given for the substituents are (except for halo)non-exhaustive and must not be construed as limiting the inventiondisclosed in this document.

“alkenyl” means an acyclic, unsaturated (at least one carbon-carbondouble bond), branched or unbranched, substituent consisting of carbonand hydrogen, for example, vinyl, allyl, butenyl, pentenyl, hexenyl,heptenyl, octenyl, nonenyl, and decenyl.

“alkenyloxy” means an alkenyl further consisting of a carbon-oxygensingle bond, for example, allyloxy, butenyloxy, pentenyloxy, hexenyloxy,heptenyloxy, octenyloxy, nonenyloxy, and decenyloxy.

“alkoxy” means an alkyl further consisting of a carbon-oxygen singlebond, for example, methoxy, ethoxy, propoxy, isopropoxy, 1-butoxy,2-butoxy, isobutoxy, tert-butoxy, pentoxy, 2-methylbutoxy,1,1-dimethylpropoxy, hexoxy, heptoxy, octoxy, nonoxy, and decoxy.

“alkyl” means an acyclic, saturated, branched or unbranched, substituentconsisting of carbon and hydrogen, for example, methyl, ethyl, propyl,isopropyl, 1-butyl, 2-butyl, isobutyl, tert-butyl, pentyl,2-methylbutyl, 1,1-dimethylpropyl, hexyl, heptyl, octyl, nonyl, anddecyl.

“alkynyl” means an acyclic, unsaturated (at least one carbon-carbontriple bond, and any double bonds), branched or unbranched, substituentconsisting of carbon and hydrogen, for example, ethynyl, propargyl,butynyl, pentynyl, hexynyl, heptynyl, octynyl, nonynyl, and decynyl.

“halo” means fluoro, chloro, bromo, and iodo.

“haloalkoxy” means a haloalkyl further consisting of a carbon-oxygensingle bond, for example, fluoromethoxy, difluoromethoxy, andtrifluoromethoxy, 2-fluoroethoxy, 1,1,2,2,2-pentafluoroethoxy,1,1,2,2-tetrafluoro-2-bromoethoxy and 1,1,2,2-tetrafluoroethoxy.

“haloalkyl” means an alkyl further consisting of, from one to themaximum possible number of, identical or different, halos, for example,fluoromethyl, difluoromethyl, trifluoromethyl, 2-fluoroethyl,2,2,2-trifluoroethyl, chloromethyl, trichloromethyl, and1,1,2,2-tetrafluoroethyl.

“halophenyloxy” means a phenyloxy having one or more, identical ordifferent, halos.

“hydroxyalkyl” means an alkyl having one or more hydroxy groups.

DETAILED DESCRIPTION OF THE INVENTION

The compounds of this invention have the following formula:

wherein:

(a) Ar₁ is

-   -   (1) furanyl, phenyl, pyridazinyl, pyridyl, pyrimidinyl, thienyl,        or    -   (2) substituted furanyl, substituted phenyl, substituted        pyridazinyl, substituted pyridyl, substituted pyrimidinyl, or        substituted thienyl,        -   wherein said substituted furanyl, substituted phenyl,            substituted pyridazinyl, substituted pyridyl, substituted            pyrimidinyl, and substituted thienyl, have one or more            substituents independently selected from H, OH, F, Cl, Br,            I, CN, NO₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆            hydroxyalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₃-C₆            hydroxycycloalkyl, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy,            C₃-C₆ hydroxycycloalkoxy, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy,            C₂-C₆ alkenyl, C₂-C₆ alkynyl, S(═O)_(n)(C₁-C₆ alkyl),            S(═O)_(n)(C₁-C₆ haloalkyl), OSO₂(C₁-C₆ alkyl), OSO₂(C₁-C₆            haloalkyl), C(═O)H, C(═O)OH, C(═O)NR_(x)R_(y), (C₁-C₆            alkyl)NR_(x)R_(y), C(═O)(C₁-C₆ alkyl), C(═O)O(C₁-C₆ alkyl),            C(═O)(C₁-C₆ haloalkyl), C(═O)O(C₁-C₆ haloalkyl), C(═O)(C₃-C₆            cycloalkyl), C(═O)O(C₃-C₆ cycloalkyl), C(═O)(C₂-C₆ alkenyl),            C(═O)O(C₂-C₆ alkenyl), (C₁-C₆ alkyl)O(C₁-C₆ alkyl), (C₁-C₆            alkyl)S(C₁-C₆ alkyl), C(═O)(C₁-C₆ alkyl)C(═O)O(C₁-C₆ alkyl),            phenyl, phenoxy, substituted phenyl and substituted phenoxy            (wherein such substituted phenyl and substituted phenoxy            have one or more substituents independently selected from H,            OH, F, Cl, Br, I, CN, NO₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl,            C₁-C₆ hydroxyalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl,            C₃-C₆ hydroxycycloalkyl, C₃-C₆ cycloalkoxy, C₃-C₆            halocycloalkoxy, C₃-C₆ hydroxycycloalkoxy, C₁-C₆ alkoxy,            C₁-C₆ haloalkoxy, C₂-C₆ alkenyl, C₂-C₆ alkynyl,            S(═O)_(n)(C₁-C₆ alkyl), S(═O)_(n)(C₁-C₆ haloalkyl),            OSO₂(C₁-C₆ alkyl), OSO₂(C₁-C₆ haloalkyl), C(═O)H, C(═O)OH,            C(═O)NR_(x)R_(y), (C₁-C₆ alkyl)NR_(x)R_(y)C(═O)(C₁-C₆            alkyl), C(═O)O(C₁-C₆ alkyl), C(═O)(C₁-C₆ haloalkyl),            C(═O)O(C₁-C₆ haloalkyl), C(═O)(C₃-C₆ cycloalkyl),            C(═O)O(C₃-C₆ cycloalkyl), C(═O)(C₂-C₆ alkenyl), C(═O)O(C₂-C₆            alkenyl), (C₁-C₆ alkyl)O(C₁-C₆ alkyl), (C₁-C₆ alkyl)S(C₁-C₆            alkyl), C(═O)(C₁-C₆ alkyl)C(═O)O(C₁-C₆ alkyl)phenyl, and            phenoxy);

(b) Het is a 5 or 6 membered, saturated or unsaturated, heterocyclicring, containing one or more heteroatoms independently selected fromnitrogen, sulfur, or oxygen, and where Ar₁ and Ar₂ are not ortho to eachother (but may be meta or para, such as, for a five membered ring theyare 1,3 and for a 6 membered ring they are either 1,3 or 1,4), and wheresaid heterocyclic ring may also be substituted with one or moresubstituents independently selected from H, OH, F, Cl, Br, I, CN, NO₂,oxo, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ hydroxyalkyl, C₃-C₆ cycloalkyl,C₃-C₆ halocycloalkyl, C₃-C₆ hydroxycycloalkyl, C₃-C₆ cycloalkoxy, C₃-C₆halocycloalkoxy, C₃-C₆ hydroxycycloalkoxy, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₂-C₆ alkenyl, C₂-C₆ alkynyl, S(═O)_(n)(C₁-C₆ alkyl),S(═O)_(n)(C₁-C₆ haloalkyl), OSO₂(C₁-C₆ alkyl), OSO₂(C₁-C₆ haloalkyl),C(═O)H, C(═O)OH, C(═O)NR_(x)R_(y), (C₁-C₆ alkyl)NR_(x)R_(y), C(═O)(C₁-C₆alkyl), C(═O)O(C₁-C₆ alkyl), C(═O)(C₁-C₆ haloalkyl), C(═O)O(C₁-C₆haloalkyl), C(═O)(C₃-C₆ cycloalkyl), C(═O)O(C₃-C₆ cycloalkyl),C(═O)(C₂-C₆ alkenyl), C(═O)O(C₂-C₆ alkenyl), (C₁-C₆ alkyl)O(C₁-C₆alkyl), (C₁-C₆ alkyl)S(C₁-C₆ alkyl), C(═O)(C₁-C₆ alkyl)C(═O)O(C₁-C₆alkyl), phenyl, phenoxy, substituted phenyl and substituted phenoxy(wherein such substituted phenyl and substituted phenoxy have one ormore substituents independently selected from H, OH, F, Cl, Br, I, CN,NO₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ hydroxyalkyl, C₃-C₆ cycloalkyl,C₃-C₆ halocycloalkyl, C₃-C₆ hydroxycycloalkyl, C₃-C₆ cycloalkoxy, C₃-C₆halocycloalkoxy, C₃-C₆ hydroxycycloalkoxy, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₂-C₆ alkenyl, C₂-C₆ alkynyl, S(═O)_(n)(C₁-C₆ alkyl),S(═O)_(n)(C₁-C₆ haloalkyl), OSO₂(C₁-C₆ alkyl), OSO₂(C₁-C₆ haloalkyl),C(═O)H, C(═O)OH, C(═O)NR_(x)R_(y), (C₁-C₆ alkyl)NR_(x)R_(y), C(═O)(C₁-C₆alkyl), C(═O)O(C₁-C₆ alkyl), C(═O)(C₁-C₆ haloalkyl), C(═O)O(C₁-C₆haloalkyl), C(═O)(C₃-C₆ cycloalkyl), C(═O)O(C₃-C₆ cycloalkyl),C(═O)(C₂-C₆ alkenyl), C(═O)O(C₂-C₆ alkenyl), (C₁-C₆ alkyl)O(C₁-C₆alkyl), (C₁-C₆ alkyl)S(C₁-C₆ alkyl), C(═O)(C₁-C₆ alkyl)C(═O)O(C₁-C₆alkyl), phenyl, and phenoxy);

(c) Ar₂ is

-   -   (1) furanyl, phenyl, pyridazinyl, pyridyl, pyrimidinyl, thienyl,        or    -   (2) substituted furanyl, substituted phenyl, substituted        pyridazinyl, substituted pyridyl, substituted pyrimidinyl, or        substituted thienyl, wherein said substituted furanyl,        substituted phenyl, substituted pyridazinyl, substituted        pyridyl, substituted pyrimidinyl, and substituted thienyl, have        one or more substituents independently selected from H, OH, F,        Cl, Br, I, CN, NO₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆        hydroxyalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₃-C₆        hydroxycycloalkyl, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy,        C₃-C₆ hydroxycycloalkoxy, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₆        alkenyl, C₂-C₆ alkynyl, S(═O)_(n)(C₁-C₆ alkyl), S(═O)_(n)(C₁-C₆        haloalkyl), OSO₂(C₁-C₆ alkyl), OSO₂(C₁-C₆ haloalkyl), C(═O)H,        C(═O)OH, C(═O)NR_(x)R_(y), (C₁-C₆ alkyl)NR_(x)R_(y), C(═O)(C₁-C₆        alkyl), C(═O)O(C₁-C₆ alkyl), C(═O)(C₁-C₆ haloalkyl),        C(═O)O(C₁-C₆ haloalkyl), C(═O)(C₃-C₆ cycloalkyl), C(═O)O(C₃-C₆        cycloalkyl), C(═O)(C₂-C₆ alkenyl), C(═O)O(C₂-C₆ alkenyl), (C₁-C₆        alkyl)O(C₁-C₆ alkyl), (C₁-C₆ alkyl)S(C₁-C₆ alkyl), C(═O)(C₁-C₆        alkyl)C(═O)O(C₁-C₆ alkyl), phenyl, phenoxy, substituted phenyl        and substituted phenoxy (wherein such substituted phenyl and        substituted phenoxy have one or more substituents independently        selected from H, OH, F, Cl, Br, I, CN, NO₂, C₁-C₆ alkyl, C₁-C₆        haloalkyl, C₁-C₆ hydroxyalkyl, C₃-C₆ cycloalkyl, C₃-C₆        halocycloalkyl, C₃-C₆ hydroxycycloalkyl, C₃-C₆ cycloalkoxy,        C₃-C₆ halocycloalkoxy, C₃-C₆ hydroxycycloalkoxy, C₁-C₆ alkoxy,        C₁-C₆ haloalkoxy, C₂-C₆ alkenyl, C₂-C₆ alkynyl, S(═O)_(n)(C₁-C₆        alkyl), S(═O)_(n)(C₁-C₆ haloalkyl), OSO₂(C₁-C₆ alkyl),        OSO₂(C₁-C₆ haloalkyl), C(═O)H, C(═O)OH, C(═O)NR_(x)R_(y), (C₁-C₆        alkyl)NR_(x)R_(y), C(═O)(C₁-C₆ alkyl), C(═O)O(C₁-C₆ alkyl),        C(═O)(C₁-C₆ haloalkyl), C(═O)O(C₁-C₆ haloalkyl), C(═O)(C₃-C₆        cycloalkyl), C(═O)O(C₃-C₆ cycloalkyl), C(═O)(C₁-C₆ haloalkyl),        C(═O)(C₂-C₆ alkenyl), C(═O)O(C₂-C₆ alkenyl), (C₁-C₆        alkyl)O(C₁-C₆ alkyl), (C₁-C₆ alkyl)S(C₁-C₆ alkyl), C(═O)(C₁-C₆        alkyl)C(═O)O(C₁-C₆ alkyl), phenyl, and phenoxy);

(d) J is O, N, NR5, CR5, C═O, or J and Ar₂ form a 3, 4, 5, or 6 memberedring, such as an indane or an indole, as, for example, in the followingstructures:

(e) L is a single or double bond;

(f) K is CR5, C═O, N, NR5, or C═S;

(g) Q is O or S;

(h) R1 is H, OH, F, Cl, Br, I, oxo, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆alkoxy, C₃-C₆ cycloalkoxy, C₁-C₆ haloalkoxy, C₂-C₆ alkenyloxy, (C₁-C₆alkyl)O(C₁-C₆ alkyl), (C₁-C₆ alkyl)O(C₁-C₆ alkoxy), OC(═O)(C₁-C₆ alkyl),OC(═O)(C₃-C₆ cycloalkyl), OC(═O)(C₁-C₆ haloalkyl), OC(═O)(C₂-C₆alkenyl), or NR_(x)R_(y);

(i) R2 is H, OH, F, Cl, Br, I, oxo, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆alkoxy, C₃-C₆ cycloalkoxy, C₁-C₆ haloalkoxy, C₂-C₆ alkenyloxy, (C₁-C₆alkyl)O(C₁-C₆ alkyl), (C₁-C₆ alkyl)O(C₁-C₆ alkoxy), OC(═O)(C₁-C₆ alkyl),OC(═O)(C₃-C₆ cycloalkyl), OC(═O)(C₁-C₆ haloalkyl), OC(═O)(C₂-C₆alkenyl), or NR_(x)R_(y);

(j) R3 is H, OH, F, Cl, Br, I, oxo, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆alkoxy, C₃-C₆ cycloalkoxy, C₁-C₆ haloalkoxy, C₂-C₆ alkenyloxy, (C₁-C₆alkyl)O(C₁-C₆ alkyl), (C₁-C₆ alkyl)O(C₁-C₆ alkoxy), OC(═O)(C₁-C₆ alkyl),OC(═O)(C₃-C₆ cycloalkyl), OC(═O)(C₁-C₆ haloalkyl), OC(═O)(C₂-C₆alkenyl), or NR_(x)R_(y);

(k) R4 is H, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₂-C₆ alkenyloxy, (C₁-C₆ alkyl)O(C₁-C₆ alkyl); and

(l) R5 is H, OH, F, Cl, Br, I, CN, NO₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl,C₁-C₆ hydroxyalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₃-C₆hydroxycycloalkyl, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₃-C₆hydroxycycloalkoxy, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₆ alkenyl, C₂-C₆alkynyl, S(═O)_(n)(C₁-C₆ alkyl), S(═O)_(n)(C₁-C₆ haloalkyl), OSO₂(C₁-C₆alkyl), OSO₂(C₁-C₆ haloalkyl), C(═O)H, C(═O)OH, C(═O)NR_(x)R_(y), (C₁-C₆alkyl)NR_(x)R_(y), C(═O)(C₁-C₆ alkyl), C(═O)O(C₁-C₆ alkyl), C(═O)(C₁-C₆haloalkyl), C(═O)O(C₁-C₆ haloalkyl), C(═O)(C₃-C₆ cycloalkyl),C(═O)O(C₃-C₆ cycloalkyl), C(═O)(C₂-C₆ alkenyl), C(═O)O(C₂-C₆ alkenyl),(C₁-C₆ alkyl)O(C₁-C₆ alkyl), (C₁-C₆ alkyl)S(C₁-C₆ alkyl), C(═O)(C₁-C₆alkyl)C(═O)O(C₁-C₆ alkyl), phenyl, phenoxy, wherein each alkyl,haloalkyl, hydroxyalkyl, cycloalkyl, halocycloalkyl, hydroxycycloalkyl,cycloalkoxy, halocycloalkoxy, hydroxycycloalkoxy, alkoxy, haloalkoxy,alkenyl, alkynyl, phenyl, and phenoxy are optionally substituted withone or more substituents independently selected from OH, F, Cl, Br, I,CN, NO₂, oxo, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ hydroxyalkyl, C₃-C₆cycloalkyl, C₃-C₆ halocycloalkyl, C₃-C₆ hydroxycycloalkyl, C₃-C₆cycloalkoxy, C₃-C₆ halocycloalkoxy, C₃-C₆ hydroxycycloalkoxy, C₁-C₆alkoxy, C₁-C₆ haloalkoxy, C₂-C₆ alkenyl, C₂-C₆ alkynyl, S(═O)_(n)(C₁-C₆alkyl), S(═O)_(n)(C₁-C₆ haloalkyl), OSO₂(C₁-C₆ alkyl), OSO₂(C₁-C₆haloalkyl), C(═O)H, C(═O)OH, C(═O)NR_(x)R_(y), (C₁-C₆ alkyl)NR_(x)R_(y),C(═O)(C₁-C₆ alkyl), C(═O)O(C₁-C₆ alkyl), C(═O)(C₁-C₆ haloalkyl),C(═O)O(C₁-C₆ haloalkyl), C(═O)(C₃-C₆ cycloalkyl), C(═O)O(C₃-C₆cycloalkyl), C(═O)(C₂-C₆ alkenyl), C(═O)O(C₂-C₆ alkenyl), (C₁-C₆alkyl)O(C₁-C₆ alkyl), (C₁-C₆ alkyl)S(C₁-C₆ alkyl), C(═O)(C₁-C₆alkyl)C(═O)O(C₁-C₆ alkyl), phenyl, and phenoxy;

(m) n=0, 1, or 2;

(n) R_(x) and R_(y) are independently selected from H, C₁-C₆ alkyl,C₁-C₆ haloalkyl, C₁-C₆ hydroxyalkyl, C₃-C₆ cycloalkyl, C₃-C₆halocycloalkyl, C₃-C₆ hydroxycycloalkyl, C₃-C₆ cycloalkoxy, C₃-C₆halocycloalkoxy, C₃-C₆ hydroxycycloalkoxy, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₂-C₆ alkenyl, C₂-C₆ alkynyl, S(═O)_(n)(C₁-C₆ alkyl),S(═O)_(n)(C₁-C₆ haloalkyl), OSO₂(C₁-C₆ alkyl), OSO₂(C₁-C₆ haloalkyl),C(═O)H, C(═O)OH, C(═O)(C₁-C₆ alkyl), C(═O)O(C₁-C₆ alkyl), C(═O)(C₁-C₆haloalkyl), C(═O)O(C₁-C₆ haloalkyl), C(═O)(C₃-C₆ cycloalkyl),C(═O)O(C₃-C₆ cycloalkyl), C(═O)(C₂-C₆ alkenyl), C(═O)O(C₂-C₆ alkenyl),(C₁-C₆ alkyl)O(C₁-C₆ alkyl), (C₁-C₆ alkyl)S(C₁-C₆ alkyl), C(═O)(C₁-C₆alkyl)C(═O)O(C₁-C₆ alkyl), phenyl, and phenoxy.

In another embodiment of this invention:

(a) Ar₁ is phenyl, pyridazinyl, pyridyl, thienyl, substituted phenyl,substituted pyridazinyl, substituted pyridyl, or substituted thienyl,wherein said substituted phenyl, substituted pyridazinyl, substitutedpyridyl, and substituted thienyl, have one or more substituentsindependently selected from F, Cl, Br, I, CN, NO₂, C₁-C₆ alkyl, C₁-C₆haloalkyl, C₁-C₆ hydroxyalkyl, C₁-C₆ haloalkoxy, C₂-C₆ alkenyl,S(═O)_(n)(C₁-C₆ alkyl), S(═O)_(n)(C₁-C₆ haloalkyl), OSO₂(C₁-C₆haloalkyl), C(═O)(C₁-C₆ alkyl), (C₁-C₆ alkyl)S(C₁-C₆ alkyl), and phenoxy(wherein such substituted phenoxy has one or more substituentsindependently selected from F, Cl, Br, or I).

In another embodiment of the invention:

(a) Ar₁ is substituted phenyl or substituted pyridyl wherein saidsubstituted phenyl and substituted pyridyl, have one or moresubstituents independently selected from F, Cl, Br, I, CN, NO₂, C₁-C₆alkyl, C₁-C₆ haloalkyl, C₁-C₆ hydroxyalkyl, C₁-C₆ haloalkoxy, C₂-C₆alkenyl, S(═O)_(n)(C₁-C₆ alkyl), S(═O)_(n)(C₁-C₆ haloalkyl), OSO₂(C₁-C₆haloalkyl), C(═O)(C₁-C₆ alkyl), (C₁-C₆ alkyl)S(C₁-C₆ alkyl), and phenoxy(wherein such substituted phenoxy has one or more substituentsindependently selected from F, Cl, Br, or I).

In another embodiment of the invention:

(a) Ar₁ is substituted phenyl wherein said substituted phenyl has one ormore substituents independently selected from F, Cl, Br, I, C₁-C₆ alkyl,C₁-C₆ haloalkyl, and C₁-C₆ haloalkoxy.

In another embodiment of the invention:

(b) Het is imidazolyl, isothiazolyl, isoxazolyl, 1,2,4-oxadiazolyl,1,3,4-oxadiazolyl, oxazolinyl, oxazolyl, piperazinyl, piperidinyl,pyrazinyl, pyrazolinyl, pyrazolyl, pyridazinyl, pyridyl, pyrimidinyl,pyrrolyl, 1,2,3,4-tetrazolyl, thiadiazolyl, thiazolinyl, thiazolyl,1,2,3-triazinyl, 1,2,4-triazinyl, 1,3,5-triazinyl, 1,2,3-triazolyl,1,2,4-triazolyl, substituted imidazolyl, substituted isothiazolyl,substituted isoxazolyl, substituted 1,2,4-oxadiazolyl, substituted 1,3,4oxadiazolyl, substituted oxazolinyl, substituted oxazolyl, substitutedpiperazinyl, substituted piperidinyl, substituted pyrazinyl, substitutedpyrazolinyl, substituted pyrazolyl, substituted pyridazinyl, substitutedpyridyl, substituted pyrimidinyl, substituted pyrrolyl, substitutedtetrazolyl, substituted thiadiazolyl, substituted thiazolinyl,substituted thiazolyl, substituted 1,2,3-triazinyl, substituted1,2,4-triazinyl, substituted 1,3,5-triazinyl, substituted1,2,3-triazolyl, and substituted 1,2,4-triazolyl, where said substitutedgroups have one or more substituents independently selected from H, OH,F, Cl, Br, I, CN, NO₂, oxo, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆hydroxyalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₃-C₆hydroxycycloalkyl, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₃-C₆hydroxycycloalkoxy, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₆ alkenyl, C₂-C₆alkynyl, S(═O)_(n)(C₁-C₆ alkyl), S(═O)_(n)(C₁-C₆ haloalkyl), OSO₂(C₁-C₆alkyl), OSO₂(C₁-C₆ haloalkyl), C(═O)H, C(═O)OH, C(═O)NR_(x)R_(y), (C₁-C₆alkyl)NR_(x)R_(y), C(═O)(C₁-C₆ alkyl), C(═O)O(C₁-C₆ alkyl), C(═O)(C₁-C₆haloalkyl), C(═O)(C₃-C₆ cycloalkyl), C(═O)O(C₃-C₆ cycloalkyl),C(═O)(C₁-C₆ haloalkyl), C(═O)(C₂-C₆ alkenyl), C(═O)O(C₂-C₆ alkenyl),(C₁-C₆ alkyl)O(C₁-C₆ alkyl), (C₁-C₆ alkyl)S(C₂-C₆ alkyl), C(═O)(C₁-C₆alkyl)C(═O)O(C₁-C₆ alkyl)phenyl, phenoxy, substituted phenyl andsubstituted phenoxy (wherein such substituted phenyl and substitutedphenoxy have one or more substituents independently selected from H, OH,F, Cl, Br, I, CN, NO₂, oxo, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆hydroxyalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₃-C₆hydroxycycloalkyl, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₃-C₆hydroxycycloalkoxy, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₆ alkenyl, C₂-C₆alkynyl, S(═O)_(n)(C₁-C₆ alkyl), S(═O)_(n)(C₁-C₆ haloalkyl), OSO₂(C₁-C₆alkyl), OSO₂(C₁-C₆ haloalkyl), C(═O)H, C(═O)OH, C(═O)NR_(x)R_(y), (C₁-C₆alkyl)NR_(x)R_(y), C(═O)(C₁-C₆ alkyl), C(═O)O(C₁-C₆ alkyl), C(═O)(C₁-C₆haloalkyl), C(═O)(C₃-C₆ cycloalkyl), C(═O)O(C₃-C₆ cycloalkyl),C(═O)(C₁-C₆ haloalkyl), C(═O)(C₂-C₆ alkenyl), C(═O)O(C₂-C₆ alkenyl),(C₁-C₆ alkyl)O(C₁-C₆ alkyl), (C₁-C₆ alkyl)S(C₁-C₆ alkyl), C(═O)(C₁-C₆alkyl)C(═O)O(C₁-C₆ alkyl)phenyl, and phenoxy).

In another embodiment of this invention:

(b) Het is imidazolyl, isoxazolyl, 1,2,4-oxadiazolyl, 1,3,4-oxadiazolyl,oxazolyl, piperazinyl, pyrazinyl, pyrazolyl, pyridazinyl, pyridyl,pyrimidinyl, pyrrolyl, 1,2,3,4-tetrazolyl, thiadiazolyl, thiazolyl,1,2,4-triazinyl, 1,3,5-triazinyl, 1,2,3-triazolyl, 1,2,4-triazolyl,substituted imidazolyl, substituted 1,3,4-oxadiazolyl, substitutedpiperazinyl, substituted pyrazolyl, substituted pyrimidinyl, andsubstituted 1,2,4-triazolyl, where said substituted groups have one ormore substituents independently selected from F, Cl, Br, I, CN, NO₂,oxo, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ hydroxyalkyl, C₁-C₆ alkoxy,C₁-C₆ haloalkoxy, C₂-C₆ alkenyl, S(═O)_(n)(C₁-C₆ alkyl), S(═O)_(n)(C₁-C₆haloalkyl), OSO₂(C₁-C₆ haloalkyl), C(═O)O(C₁-C₆ alkyl), and (C₁-C₆alkyl)S(C₁-C₆ alkyl),

In another embodiment of this invention:

(b) Het is imidazolyl, isoxazolyl, 1,2,4-oxadiazolyl, pyrazinyl,pyrimidinyl, thiazolyl, 1,3,5-triazinyl, 1,2,4-triazolyl, substitutedimidazolyl, substituted pyrazolyl, and substituted 1,2,4-triazolyl,where said substituted groups have one or more substituentsindependently selected from oxo, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₂-C₆alkenyl, and C(═O)O(C₁-C₆ alkyl),

In another embodiment of this invention:

(c) Ar₂ is phenyl, pyridazinyl, pyridyl, thienyl, substituted phenyl,substituted pyridazinyl, substituted pyridyl, or substituted thienyl,wherein said substituted phenyl, substituted pyridazinyl, substitutedpyridyl, and substituted thienyl, have one or more substituentsindependently selected from F, Cl, Br, I, CN, NO₂, C₁-C₆ alkyl, C₁-C₆haloalkyl, C₁-C₆ hydroxyalkyl, C₁-C₆ haloalkoxy, C₂-C₆ alkenyl,S(═O)_(n)(C₁-C₆ alkyl), S(═O)_(n)(C₁-C₆ haloalkyl), OSO₂(C₁-C₆haloalkyl), C(═O)(C₁-C₆ alkyl), (C₁-C₆ alkyl)S(C₁-C₆ alkyl), and phenoxy(wherein such substituted phenoxy has one or more substituentsindependently selected from F, Cl, Br, or I).

In another embodiment of the invention:

(c) Ar₂ is substituted phenyl or substituted pyridyl wherein saidsubstituted phenyl and substituted pyridyl, have one or moresubstituents independently selected from F, Cl, Br, I, CN, NO₂, C₁-C₆alkyl, C₁-C₆ haloalkyl, C₁-C₆ hydroxyalkyl, C₁-C₆ haloalkoxy, C₂-C₆alkenyl, S(═O)_(n)(C₁-C₆ alkyl), S(═O)_(n)(C₁-C₆ haloalkyl), OSO₂(C₁-C₆haloalkyl), C(═O)(C₁-C₆ alkyl), (C₁-C₆ alkyl)S(C₁-C₆ alkyl), and phenoxy(wherein such substituted phenoxy has one or more substituentsindependently selected from F, Cl, Br, or I).

In another embodiment of the invention:

(c) Ar₂ is substituted phenyl wherein said substituted phenyl has one ormore substituents independently selected from F, Cl, Br, I, C₁-C₆ alkyl,C₁-C₆ haloalkyl, and C₁-C₆ alkoxy.

In another embodiment of this invention:

(d) J is NR5, CR5, or C═O.

In another embodiment of this invention:

(f) K is C═O, N, NR5, or C═S.

In another embodiment of this invention:

(h) R1 is H or C₁-C₆ alkoxy.

In another embodiment of this invention:

(i) R2 is H, C₁-C₆ alkoxy or C₂-C₆ alkenyloxy.

In another embodiment of this invention:

(j) R3 is C₁-C₆ alkoxy.

In another embodiment of this invention:

(k) R4 is H, C₁-C₆ alkyl, C₁-C₆ alkoxy, or (C₁-C₆ alkyl)O(C₁-C₆ alkyl).

In another embodiment of this invention:

(l) R5 is H, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ hydroxyalkyl, C₂-C₆alkenyl, C(═O)(C₁-C₆ alkyl), (C₁-C₆ alkyl)O(C₁-C₆ alkyl), andC(═O)(C₁-C₆ alkyl)C(═O)O(C₁-C₆ alkyl).

In another embodiment of this invention:

(1) R5 is H, C₁-C₆ alkyl, C₁-C₆ alkoxy, or C₁-C₆ haloalkyl.

In another embodiment of the invention:

(a) Ar₁ is phenyl, pyridyl, thienyl, substituted phenyl, substitutedpyridazinyl, or substituted pyridyl,

-   -   wherein said substituted phenyl has one or more substituents        independently selected from F, Cl, Br, I, CN, CH₃, C₃H₇, C₄H₉,        OCH₃, OC₄H₉, CF₃, C₂F₅, C₃F₇, OCF₃, OC₂F₅, OCH₂CF₃, OCF₂CHF₂,        SCF₃, SCH₃, S(═O)CF₃, S(═O)₂CF₃, OPhCl, and C(OH)C₂H₅;    -   wherein said substituted pyridazinyl has one or more Cl,    -   wherein said substituted pyridyl has one or more substituents        independently selected from F, Cl, I, CF₃, OCF₃, OCF₂CHFCF₃, and        OCH₂CF₃.

In another embodiment of this invention:

(b) Het is imidazolyl, isoxazolyl, 1,3,4-oxadiazolyl, pyrazinyl,pyrazolinyl, pyrazolyl, pyridyl, pyrimidinyl, pyrrolyl,1,2,3,4-tetrazolyl, thiazolyl, 1,3,5-triazinyl, 1,2,3-triazolyl,1,2,4-triazolyl, substituted pyrazolinyl, substituted pyrimidinyl, orsubstituted 1,2,4-triazolyl,

-   -   wherein said substituted pyrazolyl has one or more substituents        independently selected from H, CH₃, C₃H₇, C(═O)OCH₃, C(═O)OC₂H₅,        and C(═O)OC₄H₉,    -   wherein said substituted pyrimidinyl has one or more        substituents independently selected from CF₃ and C₃F₇,    -   wherein said substituted 1,2,4-triazolyl has one or more        substituents selected from CH₃ and oxo.

In another embodiment of this invention:

(c) Ar₂ is phenyl, thienyl, or substituted phenyl,

-   -   wherein said substituted phenyl has one or more substituents        independently selected from F, Cl, OCH₃, and CF₃.

In another embodiment of this invention:

(d) J is NH, CH, CCH₃, or C═O.

In another embodiment of this invention:

(h) R1 is OCH₃ or OC₂H₅.

In another embodiment of this invention:

(i) R2 is OCH₂CH═CH₂, OCH₃, OC₂H₅, OC₃H₇, or OC₄H₉.

In another embodiment of this invention:

k) R3 is OH, OCH₃, OC₂H₅, or OC₃H₇;

In another embodiment of this invention:

(k) R4 is CH₃ or CH₂OCH₃.

In another embodiment of this invention:

(a) Ar₁ is furanyl, phenyl, pyridazinyl, pyridyl, pyrimidinyl, thienyl,substituted furanyl, substituted phenyl, substituted pyridazinyl,substituted pyridyl, substituted pyrimidinyl, or substituted thienyl,wherein said substituted furanyl, substituted phenyl, substitutedpyridazinyl, substituted pyridyl, substituted pyrimidinyl, andsubstituted thienyl, have one or more substituents independentlyselected from H, F, Cl, Br, I, CN, NO₂, oxo, C₁-C₆ alkyl, C₂-C₆ alkenyl,C₂-C₆ alkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkyl, C₁-C₆ haloalkoxy,S(═O)_(n)C₁-C₆ alkyl, S(═O)_(n)C₁-C₆ haloalkyl, OSO₂C₁-C₆ haloalkyl,C(═O)OC₁-C₆ alkyl, C(═O)C₁-C₆ alkyl, C(═O)C₁-C₆ haloalkyl, phenyl,phenoxy, halophenoxy, and C₁-C₆ hydroxyalkyl;

(b) Het is a 5 or 6 membered, saturated or unsaturated, heterocyclicring, containing one or more heteroatoms independently selected fromnitrogen, sulfur, or oxygen, and where Ar₁ and Ar₂ are not ortho to eachother (but may be meta or para, such as, for a five membered ring theyare 1,3, and for a 6 membered ring they are either 1,3 or 1,4respectively), and where said heterocyclic ring may also be substitutedwith one or more substituents independently selected from H, F, Cl, Br,I, CN, NO₂, oxo, C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₁-C₆alkoxy, C₁-C₆ haloalkyl, C₁-C₆ haloalkoxy, S(═O)_(n)C₁-C₆ alkyl,S(═O)_(n)C₁-C₆ haloalkyl, OSO₂C₁-C₆ haloalkyl, C(═O)OC₁-C₆ alkyl,C(═O)C₁-C₆ alkyl, C(═O)C₁-C₆ haloalkyl, phenyl, phenoxy, halophenoxy,and C₁-C₆ hydroxyalkyl;

(c) Ar₂ is furanyl, phenyl, pyridazinyl, pyridyl, pyrimidinyl, thienyl,substituted furanyl, substituted phenyl, substituted pyridazinyl,substituted pyridyl, substituted pyrimidinyl, or substituted thienyl,wherein said substituted furanyl, substituted phenyl, substitutedpyridazinyl, substituted pyridyl, substituted pyrimidinyl, andsubstituted thienyl, have one or more substituents independentlyselected from H, F, Cl, Br, I, CN, NO₂, oxo, C₁-C₆ alkyl, C₂-C₆ alkenyl,C₂-C₆ alkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkyl, C₁-C₆ haloalkoxy,S(═O)_(n)C₁-C₆ alkyl, S(═O)_(n)C₁-C₆ haloalkyl, OSO₂C₁-C₆ haloalkyl,C(═O)OC₁-C₆ alkyl, C(═O)C₁-C₆ alkyl, C(═O)C₁-C₆ haloalkyl, phenyl,phenoxy, halophenoxy, and C₁-C₆ hydroxyalkyl;

(d) J is O, N, NR5, CR5, or C═O;

(e) L is a single or double bond;

(f) K is CR5, C═O, N, NR5, or C═S;

(g) Q is O or S;

(h) R1 is C₁-C₆ alkyl, C₁-C₆ alkyl-O—C₁-C₆ alkyl, C₁-C₆ haloalkyl, halo,oxo, C₁-C₆ haloalkoxy, C₁-C₆ alkyl-O—C₁-C₆ alkoxy, H, OH, C₁-C₆ alkoxy,C₂-C₆ alkenyloxy;

(i) R2 is C₁-C₆ alkyl, C₁-C₆ alkyl-O—C₁-C₆ alkyl, C₁-C₆ haloalkyl, halo,oxo, C₁-C₆ haloalkoxy, C₁-C₆ alkyl-O—C₁-C₆ alkoxy, H, OH, C₁-C₆ alkoxy,C₂-C₆ alkenyloxy;

(j) R3 is C₁-C₆ alkyl, C₁-C₆ alkyl-O—C₁-C₆ alkyl, C₁-C₆ haloalkyl, halo,oxo, C₁-C₆ haloalkoxy, C₁-C₆ alkyl-O—C₁-C₆ alkoxy, H, OH, C₁-C₆ alkoxy,C₂-C₆ alkenyloxy;

(k) R4 is C₁-C₆ alkyl, C₁-C₆ alkyl-O—C₁-C₆ alkyl, C₁-C₆ haloalkyl, H,C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₆ alkenyloxy

(l) R5 is H or C₁-C₆ alkyl; and

(m) n=0, 1, or 2.

While these embodiments have been expressed, other embodiments andcombinations of these expressed embodiments and other embodiments, arepossible.

Preparation of Pyranose-Intermediates

A wide variety of pyranoses (in different structural forms, for example,D and L) can be used to make the compounds of this invention. Forexample, the following non-exhaustive list of pyranoses may be used:ribose, arabinose, xylose, lyxose, ribulose, xylulose, allose, altrose,glucose, mannose, gulose, idose, galactose, talose, psicose, fructose,sorbose, tagatose, fucose, mycarose, quinovose, oleandrose, rhamnose,and paratose. In most of the examples below, L-rhamnose was used to makepyranose-intermediates.

In general, pyranose-intermediates can be made as follows (usingL-rhamnose as an example). O-alkylated rhamnose derivatives can beprepared from commercially available L-rhamnose or L-rhamnose hydrate byusing an alkyl iodide and powdered potassium hydroxide in dry dimethylsulfoxide (DMSO) at from 5° C. to 15° C. The fully alkylated product isthen isolated by extraction of the dimethyl sulfoxide solution withhexanes, followed by concentration of the hexane layer under vacuum.This intermediate alkyl pyranoside is then treated directly with aqueousHCl or other aqueous acid, which forms the free hydroxy sugar, usuallyas a mixture of α- and β-anomers.

Alternatively, the per-alkylated L-rhamnose can be isolated byhydrolysis of spinosad or other tri-(O-alkyl)rhamnosylated naturalproduct, using conditions similar to those described for the isolationof methyl oleandroside from avermectin B₂ (Loewe et al. J. Org. Chem.1994, 59, 7870). Thus, treatment of technical spinosad with excessconcentrated sulfuric acid in dry methanol (MeOH) results in hydrolysisof the rhamnose sugar and conversion into the methyl pyranoside. Thepure methylpyranoside can then be removed from the reaction medium byexhaustive extraction with hexanes or other hydrocarbon solvent. Thepure rhamnopyranoside can then be isolated in ca. 65-75% overall yieldby distillation of the crude liquor under vacuum.

The 3-O-ethyl-2,4-di-O-methyl rhamnose can be prepared in a similarmanner, starting from spinetoram. Other alkylated derivatives can belikewise produced by starting with the appropriately functionalizedspinosoid derivatives, which are made from any spinosyn factor which hasone or more free hydroxyl groups attached to rhamnose (for example,spinosyn J) using conditions described in DeAmicis et al. U.S. Pat. No.6,001,981, 1999.

A rhamnose precursor that is selectively alkylated with a largersubstituent at C3 has been described (see, for example, Pozsgay et al.Can. J. Chem. 1987, 65, 2764). An alternate route, which avoids the useof tin reagents, is described below. Reaction of the methylpyranoside ofL-rhamnose with one equivalent of phenylboronic acid, ortriphenylboroxole, under conditions that allow for removal of water,results in formation of a boron acetal. Treatment of this acetal with analkyl halide and silver oxide, in a polar aprotic solvent such asdimethyl formamide, at from 0° C. to 110° C. results in a selectivealkylation at C3-OH, giving the 3-O-alkyl methylpyranoside. Thismaterial can then be further methylated at positions 2-OH and 4-OH withmethyl iodide, using conditions described previously. The fullyalkylated rhamnose can then be hydrolyzed as described above to give2,4-di-O-methyl-3-O-alkyl-L-rhamnose.

Illustrations of making such pyranose-intermediates are given in theexamples.

Hydroxylamino pyranose-intermediates can also be made. For example, theycan be prepared from the corresponding rhamnose derivative and N-hydroxysuccinimide (NHS) under conditions in which the water formed is removedazeotropically, to form an N-succinimidoyl hydroxylamine adduct. In oneembodiment, these conditions involve combining rhamnose and NHS intoluene or benzene, adding a catalytic amount of an acid such asp-toluenesulfonic acid (TsOH), and heating to reflux in an apparatusequipped with a Dean-Stark trap. Conversion to the free hydroxylamineintermediate is accomplished by treatment of the succinimidoyl adductwith excess hydrazine hydrate or anhydrous hydrazine in an alcoholicsolvent such as methanol (MeOH) or ethanol (EtOH). Reaction of theO-rhamnosyl hydroxylamine with an aldehyde or ketone using EtOH or otherlower alcohol solvent at from ambient temperature to reflux thenproduces an O-rhamnosyl oxime.

Preparation of Triaryl-Intermediates

Compounds of this invention are prepared by linking the above-describedpyranoses to a triaryl intermediate, Ar₁-Het-Ar₂, by means of a covalentlinker J[L]KQ (defined above). A wide variety of triaryl precursors canbe used to prepare compounds of this invention, provided that theycontain a suitable functional group on Ar₂ to which the pyranoseintermediate can be attached in order to form the covalent linker.Suitable functional groups include an amino, oxoalkyl, formyl, orcarboxylic acid group. These triaryl-intermediates can be prepared bymethods previously described in the chemical literature. Several ofthese methods are described below.

Intermediates wherein ‘Het’ is a disubstituted pyridine, pyrimidine,pyrazine or pyridizine can be made by coupling of a halo- oralkylthio-substituted pyridine, pyrimidine or pyrazine with an arylboronic acid or borate ester, under Suzuki arylation conditions. See,for example, the following.

For pyridines: Couve-Bonnaire et al. Tetrahedron 2003, 59, 2793 andPuglisi et al. Eur, J. Org. Chem. 2003, 1552.

For pyrazines: Schultheiss and Bosch Heterocycles 2003, 60, 1891.

For pyrimidines: Qing et al. J. Fluorine Chem. 2003, 120, 21 and Ceideand Montalban Tetrahedron Lett. 2006, 47, 4415.

For 2,4-diaryl pyrimidines: Schomake rand Delia, J. Org. Chem. 2001, 66,7125.

Thus, successive palladium-catalyzed arylations, using 4-formylphenylboronic acid and 4-trifluoromethoxyphenyl boronic acid, can generatevirtually any particular substitution pattern, as shown in the schemebelow:

Similarly, diaryl pyridines and pyrazines and other dihalogenatedheterocyclic aromatic compounds can be prepared from dihalogenatedpyridines and pyrazines and other dihalogenated heterocyclic aromaticcompounds using the same protocol:

The halo- or alkylthio-pyrimidine and pyridine precursors are eithercommercially available, or may be synthesized by routes described in theliterature (Rorig and Wagner U.S. Pat. No. 3,149,109, 1964; Kreutzbergerand Tesch Arzneim.-Forsch. 1978, 28, 235).

Compounds where ‘Het’ is a 1,3-diaryl-6-perfluoroalkyl pyrimidine can beprepared according to the following scheme. The 2-methylthio substitutedpyrimidine was arylated under modified Suzuki conditions (Liebeskind andSrogl Org. Lett. 2002, 4, 979) to give 2-phenyl pyrimidines, which thenwere reduced to the corresponding anilines using, for example, a Pd/Ccatalyst in EtOH under hydrogen atmosphere.

Intermediate compounds wherein ‘Het’ is a 1,3-disusbstituted1,2,4-triazole can be prepared according to one of the followingschemes.

Route A: 1,3-diaryl 1,2,4-triazoles were prepared from the corresponding—NH 3-aryl 1,2,4-triazoles by following a published route forN-arylation of imidazoles (Lin et al. J. Org. Chem. 1979, 44, 4160).Coupling of 1,2,4-triazoles to aryl halides was done under thermal or,preferably, microwave conditions (Antilla et al. J. Org. Chem. 2004, 69,5578). (DIBAL is diisobutylaluminum hydride.)

Route B: Bromination of hydrazones followed by treatment of thebromohydrazone with tetrazole results in formation of the 1,3-diaryl1,2,4-triazole (Butler and Fitzgerald J. Chem. Soc., Perkin Trans.11988, 1587).

Route C. 1,2,4-Triazole compounds in which the 5-position is furthersubstituted with an alkyl or substituted alkyl group can be preparedaccording to the following scheme (Paulvannan and Hale Tetrahedron 2000,56, 8071):

Compounds where ‘Het’ is an imidazole can be prepared according to oneof the following schemes:

Route A (Step 1: Lynch et al. J. Am. Chem. Soc. 1994, 116, 11030. Step2: Liu et al. J. Org. Chem. 2005, 70, 10135):

Route B. For halo-aryl groups that also contain an activating group suchas nitro or cyano, displacement of an aryl halide with an imidazole,using a base such as potassium carbonate in a polar aprotic solvent suchas N,N-dimethylformamide (DMF) or dimethyl sulfoxide (DMSO) can beaccomplished in the following manner (Bouchet et al., Tetrahedron 1979,35, 1331):

Route C: Following a procedure first described by Porretta et al.(Farmaco, Edizione Scientifica 1985, 40, 404), an N-phenacyl aniline istreated with potassium thiocyanate in acidic medium (HCl), and theresulting 2-mercapto imidazole is then converted into the desulfurizeddiaryl imidazole by treatment with nitric acid in acetic acid.

Route D. N-Arylation of 4-bromoimidazole under microwave irradiationconditions (Route A, Step 2) furnished the intermediate1-aryl-4-bromoimidazole, which was converted into triaryl-intermediatesby treatment with aryl boronic acids under palladium-catalyzedconditions.

Compounds where ‘Het’ is a 1,4-disubstituted 1,2,3-triazole can beprepared according to the following scheme (Feldman et al. Org. Lett.2004, 6, 3897):

Compounds where ‘Het’ is a 3,5-disubstituted 1,2,4-triazole can beprepared according to the following scheme (Yeung et al. TetrahedronLett. 2005, 46, 3429):

Compounds where ‘Het’ is a 1,3-disubstituted 1,2,4-triazolin-5-one canbe prepared according to the following scheme (Pirrung and Tepper J.Org. Chem. 1995, 60, 2461 and Lyga Synth. Commun. 1986, 16, 163). (DPPAis diphenyl phosphoryl azide.):

Compounds where ‘Het’ is a 1,3-diaryl pyrazoline can be preparedaccording to the following scheme. The monohydrazone ofterephthalaldehyde is treated with NCS in i-PrOH, and the resultingchlorohydrazone intermediate is treated directly with base and asubstituted olefin to generate the pyrazoline:

Compounds where ‘Het’ is a 3,5-disubstituted isoxazole can be preparedaccording to the following scheme:

Compounds where ‘Het’ is a 1,3-disubstituted pyrazole can be preparedaccording to the following scheme. Coupling of the pyrazole tohalogenated aromatics was accomplished using microwave conditionsdescribed by Liu et al., Route A, Step 2 above. (DMA is dimethylacetal.)

Compounds where ‘Het’ is a 2,4-disubstituted thiazole are prepared bycondensation of a thioamide to an α-halo acetophenone in a proticsolvent such as ethanol (for example, Potts and Marshall J. Org. Chem.1976, 41, 129).

Compounds where ‘Het’ is a 1,4-disubstituted 1,2,4-triazolin-5-one areprepared according to the following scheme (Henbach DE 2724819 A1, 1978with slight modification to two steps):

Compounds where ‘Het’ is a 2,4-disubstituted oxazoline are preparedstarting from the α-bromoacetophenone according to the following scheme(Periasamy et al. Synthesis 2003, 1965 and Liu et al. J. Am. Chem. Soc.2007, 129, 5834).

Compounds where ‘Het’ is a 2,5-disubstituted oxazoline are preparedaccording to the following scheme (Favretto et al. Tetrahedron Lett.2002, 43, 2581 and Liu et al. J. Am. Chem. Soc. 2007, 129, 5834):

Compounds where ‘Het’ is a 1,4-disubstituted piperazine are preparedaccording to the following scheme (Evans et al. Tetrahedron Lett. 1998,39, 2937):

Compounds where ‘Het’ is a 1,3-disubstituted pyrazoline are prepared byaddition of an aryl hydrazine to a β-dimethylamino propiophenone asshown in the following scheme, which is described in Linton et al.Tetrahedron Lett. 2007, 48, 1993, and Wheatley et al. J. Am. Chem. Soc.1954, 76, 4490. In addition to the pyrazoline, a minor amount ofbis-addition leads to the corresponding dimethylaminomethyl pyrazoline.These materials can be separated chromatographically.

Compounds where ‘Het’ is a 3,5-disubstituted 1,2,4-triazine are preparedaccording to the following scheme (Reid et al. Bioorg. Med. Chem. Lett.2008, 18, 2455 and Saraswathi and Srinivasan Tetrahedron Lett. 1971,2315):

Compounds where ‘Het’ is a 2-ketopiperazine or 2,5-diketopiperazine areprepared as in the following scheme. The nitrophenyl glycine ester canbe acylated using chloroacetyl chloride, and the intermediateN-chloroacetylated glycine ester, upon treatment with an aniline,undergoes displacement and ring closure at from 120 to 180° C. to form adiketopiperazine. Alternatively, monoketo saturated or unsaturatedpiperazines can be formed from the acetal intermediate below, byhydrolysis and ring closure.

Preparation of Oxime-Linked Compounds

Oxime-linked compounds can be prepared from the corresponding arylaldehydes or ketones by reaction with the corresponding 2-hydroxylaminosugar, in an organic solvent such as MeOH or EtOH, at temperaturesbetween 0 and 100° C.

Preparation of (Thio)Carbamate-Linked Compounds

Carbamate- or thio-carbamate linked compounds can be prepared from thecorresponding aryl amines by conversion into either an isocyanate,isothiocyanate or p-nitrophenyl carbamate, followed by treatment withthe appropriate alcohol (ROH) and an organic or inorganic base in asuitable solvent such as tetrahydrofuran (THF), at temperatures between0 and 100° C.

Alternatively, an isocyanate intermediate can be generated from thecarboxylic acid by treating with a source of azide such asdiphenylphosphoryl azide (DPPA). The acyl azide then can be made toundergo a Curtius rearrangement by heating to 110° C. in toluene, andthe resulting isocyanate treated with an appropriate sugar and a base asdescribed above to generate the carbamate.

In these reactions, the α-configuration at Cl of the rhamnose moiety isusually the major product, although a minor amount of the β-anomer isalso formed. These two isomers may be separated by chromatography, orthey may be used as a mixture.

Carbamates can also be prepared via nitrophenyl carbonates as shownlater. It is advantageous to treat the pyrimidinylaniline first with astrong base such as lithium or potassium hexamethlydisilazide (HMDS)followed by the nitrophenyl carbonate. The p-nitrophenyl carbonate canbe prepared by reaction of the tri-O-methylrhamnose hemi-acetal withp-nitrophenyl chloroformate in pyridine/dioxane.

Thio-carbamate derivatives can be prepared from the S-alkyl rhamnose,which is generated from the rhamnosyl pyranoside by treatment withLawesson's reagent (Bernardes et al. Angew. Chem. Int. Ed. 2006, 45,4007). Treatment of the glycosyl thiol with an isocyanate orp-nitrophenyl carbamate and an organic base such as triethylaminefurnishes the thiocarbamate.

Preparation of Hydroxamate-Linked Compounds

Hydroxamic ester-linked compounds can be prepared by treatment of anacid chloride with the hydroxylamine and an organic base such astriethylamine:

Preparation of compounds within the scope of this invention can be doneby the synthesis of an appropriate triaryl intermediate containing anacid, aldehyde, ketone, or amino functional group for attachment to thepyranose-intermediate.

EXAMPLES

These examples are for illustration purposes and are not to be construedas limiting the invention disclosed in this document to only theembodiments disclosed.

Example 1 Preparation of(3R,4R,5S,6S)-2,3,4,5-tetramethoxy-6-methyl-tetrahydropyran (CompoundE-1)

A solution of L-rhamnose hydrate (40 g, 0.22 mol) in 450 mL of drydimethyl sulfoxide was placed in a 2 L 3-neck round bottom flask andstirred mechanically while powdered KOH (75 g, 1.34 mol) was added inone portion. Iodomethane (187 g, 1.32 mol) was added to this solution ata rate such that the temperature of the solution was maintained below30° C. A dry ice-acetone bath was used intermittently to maintain thistemperature. After the addition was complete (about 2 h), the solutionwas stirred an additional 3 h, then it was allowed to stand at ambienttemperature overnight. This clear solution was then extracted with 4×500mL of hexanes, and the combined hexane solution was washed with brinebefore drying and evaporation of solvent. There was obtained 44 g (92%)of a light orange solution. Distillation gave 40 g of a colorless oil,bp 150° C. (0.5 mm Hg).

Example 2 Preparation of(3R,4R,5S,6S)-3,4,5-trimethoxy-6-methyl-tetrahydropyran-2-ol (CompoundE-2)

A solution of 35.7 g (0.162 mol) of E-1 in 300 mL of 2 N hydrochloricacid was heated at 98° C. for 5 h, was then cooled to room temperature,and was extracted with four 170-mL portions of dichloromethane (DCM).The combined extracts were dried over magnesium sulfate and decolorizedwith charcoal. Concentration gave 24.7 g (74%) of the titled compound asa viscous oil. A portion of the crude product (960 mg) was vacuumdistilled using a Kuhgelrohr apparatus collecting 890 mg at 145-155° C.(1-2 mm).

Example 3 Preparation of(3R,4R,5S,6S)-4-ethoxy-2,3,5-trimethoxy-6-methyl-tetrahydropyran(Compound E-3)

Sulfuric acid (300 mL, 98%, 5.6 mol) was added slowly to a stirredsolution of 2.5 L of methanol in a 4 L Erlenmeyer flask. When thesolution had cooled to ambient temperature, 3′-OEt spinosyn J/L (350 g,0.47 mol, prepared as in DeAmicis et al., U.S. Pat. No. 6,001,981, 1999)was added and the resulting solution was heated at reflux for 6 h. Thecooled solution was transferred to a 4 L separatory funnel and extractedwith 3×1 L of hexanes. The combined organic solution was dried andconcentrated in vacuo, then distilled using a Kugelrohr apparatus. Therewas obtained 65 g (60%) of colorless oil, bp 165° C. (10 mTorr).

Example 4 Preparation of(2R,3R,4R,5S,6S)-2,3,5-trimethoxy-6-methyl-4-propoxy-tetrahydropyran(Compound E-5)

Step 1.(2R,3R,4R,5R,6S)-2-Methoxy-6-methyl-4-propoxy-tetrahydropyran-3,5-diol.Following the procedure described by Aoyama et al. (Tetrahedron Lett.1997, 38, 5001) for preparation of the 3,4-boronate ester of methylα-L-fucopyranoside, methyl α-L-rhamnopyranoside was converted into the2,3-boronate ester. The crude ester (10.0 g, 37.7 mmol) was dissolved in150 mL of toluene and treated with iodopropane (8.0 g, 47 mmol), silveroxide (21.8 g, 94.3 mmol) and triethylamine (4.77 g, 47.1 mmol). Thesolution was heated to 100° C. and allowed to stir overnight (16 h).After cooling and filtering, the solution was concentrated to a gummyoil and was purified by silica gel chromatography eluting with anEtOAc-hexane gradient to obtain 5.9 g of pure product.

Step 2. The material from Step 1 was methylated using MeI and KOH, underconditions described in Example 1 to furnish compound E-4.

The pyranose-intermediates listed in Table 1 (Compounds E-1 throughE-E-22) were prepared by the routes described earlier and illustrated inExamples 1-4.

An example of the preparation of 2-O-succinimidoylpyranose-intermediates is described below.

Example 5 Preparation of1-((2S,3R,4R,5S,6S)-3,4,5-trimethoxy-6-methyl-tetrahydropyran-2-yloxy)-pyrrolidine-2,5-dione(Compound E-23)

To a stirred solution of 2,3,4-tri-O-methyl-L-rhamnose (6.5 g, 31.5mmol) and N-hydroxysuccinimide (5.4 g, 47 mmol) in 50 mL of benzene wasadded 50 mg (cat) of p-toluenesulfonic acid. The solution was heated toreflux and water was collected using a Dean-Stark trap. After 4 h, thesolution was cooled and the supernatant toluene layer was separated froma small amount of insoluble gum. The organic layer was washed with 20 mLof saturated NaHCO₃ solution, then dried over MgSO₄ and concentrated toa solid. Recrystallization from ether-hexanes gave 4.95 g (52%) of thetitle compound as an off-white solid.

Example 6 Preparation of1-((2S,3R,4R,5S,6S)-5-hydroxy-3,4-dimethoxy-6-methyl-tetrahydropyran-2-yloxy)-pyrrolidine-2,5-dione(Compound E-24)

A solution of(2R,3R,4R,5S,6S)-5-benzyloxy-3,4-dimethoxy-6-methyl-tetrahydropyran-2-ol(10.5 g, 26.6 mmol, prepared according to Wu et al. Carbohydr. Res.1998, 306, 493), N-hydroxysuccinimide (5.0 g, 50 mmol) and TsOH (250 mg,cat.) in 100 mL of benzene was heated at reflux for 24 h with removal ofwater using a Dean-Stark trap. The brown solution was cooled, filtered,washed with saturated sodium bicarbonate solution and concentrated. Thegummy oil was purified by chromatography on silica gel, eluting with70:30 hexanes:acetone. The pure O-succinimide (7.5 g, 14.5 mmol) wasthen transferred to a 500 mL Parr hydrogenation apparatus anddebenzylated using 0.95 g of Pd(OH)₂/C in 75 mL of EtOH. The solution,which took up 19 psi of hydrogen over 24 h, was then filtered andconcentrated, leaving a solid residue which was recrystallized from EtOHto give 3.25 g of a white solid.

The O-succinimidyl pyranose-intermediates listed in Table 2 (CompoundsE-23 through E-29) were prepared by the routes described earlier andillustrated in Examples 5 and 6.

An example of the preparation of 2-hydroxylamino pyranose-intermediatesfrom the corresponding O-succinimidoyl pyranose-intermediates isdescribed next.

Example 7 Preparation ofO-((2S,3R,4R,5S,6S)-3,4,5-trimethoxy-6-methyl-tetrahydropyran-2-yl)-hydroxylamine(Compound E-30)

The 2,3,4-tri-O-methyl-N-succinimidyl rhamnose derivative E-23 (0.50 g,1.6 mmol), prepared according to Example 5 was dissolved in 5 mL ofabsolute EtOH and treated with an excess of hydrazine hydrate (0.4 g, 8mmol). The solution was allowed to stir at ambient temperature for 60min, whereupon a voluminous white precipitate formed. An additional 5 mLof EtOH was added, and the solution was stirred at ambient temperatureovernight. The solution was filtered and concentrated, then purified bychromatography (100% EtOAc) to furnish E-30 as a crystalline solid.

The pyranose-intermediates in Table 3 (Compounds E-30 through E-38) wereprepared by the routes described earlier and as illustrated in Example7.

Examples 8-63 illustrate the preparation of additional molecules usefulin making various embodiments of this invention.

Example 8 Preparation of4-[1-(4-trifluoromethoxyphenyl)-1H-pyrrol-3-yl]-benzaldehyde

Step 1. 1-(4-Trifluoromethoxyphenyl)-1H-pyrrole. The compound wasprepared according to Colotta et al. J. Med. Chem. 2006, 49, 6015. Asolution of 4-trifluoromethoxyphenyl amine (500 mg, 2.82 mmol, 1.00 eq)and 2,5-diethoxy tetrahydrofuran (452 mg, 2.82 mmol, 1.00 eq) in glacialacetic acid (20 mL) was heated at 90° C. for 1 h before being dried ontosilica gel. The residue was then slurried in refluxing hexane, filteredhot, and concentrated to dryness affording the desired intermediate (519mg, 81%).

Step 2. 3-Bromo-1-(4-trifluoromethoxyphenyl)-1H-pyrrole. The compoundwas prepared according to Bray et al. J. Org. Chem. 1990, 55, 6317.

To a solution of 1-(4-trifluoromethoxyphenyl)-1H-pyrrole (519 mg, 2.29mmol, 1.00 eq) in THF (250 mL) at −78° C. was added a 0.05 M solution ofN-bromosuccinimide (408 mg, 2.29 mmol, 1.00 eq) in THF over 45 min. Thevessel was slowly warmed to room temperature before concentration toafford the crude bromopyrrole, which was shown to consist of 55% desiredintermediate by GC/MS. The material was used in the subsequent reactionwithout further purification.

Step 3. 4-[1-(4-Trifluoromethoxyphenyl)-1H-pyrrol-3-yl]-benzaldehyde. Asuspension of crude 3-bromo-1-(4-trifluoromethoxyphenyl)-1H-pyrrole (356mg, 1.26 mmol, 1.00 eq), 4-formylphenylboronic acid (283 mg, 1.89 mmol,1.50 eq), bis(triphenylphosphine)palladium(II) dichloride (27 mg, 0.04mmol, 0.03 eq), 2 M Na₂CO₃ (aq) (1.26 mL, 2.52 mmol, 2.0 eq), and1,4-dioxane (5 mL) were heated at 150° C. in a microwave reaction vesselfor 45 min. The cooled solution was then diluted with EtOAc (20 mL),filtered over Celite®, concentrated to dryness, and purified viachromatography (2:2:1, hexane:EtOAc:acetone) to afford the desiredintermediate (79 mg, 21%).

Example 9 Preparation of4-[1-(4-trifluoromethoxyphenyl)-4,5-dihydro-1H-pyrazol-3-yl]-benzaldehyde

Step 1. 1-(4-Trifluoromethoxyphenyl)-pyrazolidin-3-one: The compound wasprepared according to Rees and Tsoi Chem. Commun. 2000, 415. Asuspension of (4-trifluoromethoxyphenyl)-hydrazine hydrochloride (300mg, 1.32 mmol, 1.00 eq), 3-chloropropionyl chloride (167 mg, 1.32 mmol,1.00 eq), and PS-DIEA (1.30 g, 5.28 mmol, 4.00 eq) in THF (20 mL) wasstirred at ambient temperature for 12 h. The solution was then filtered,concentrated to dryness, and purified via chromatography (2:2:1,hexane:EtOAc:acetone) to afford the desired intermediate (120 mg, 37%).

Step 2. 3-Chloro-1-(4-trifluoromethoxyphenyl)-4,5-dihydro-1H-pyrazole:The general procedure was taken from Wang et al. Tetrahedron Lett. 2005,46, 2631. To a solution of1-(4-trifluoromethoxyphenyl)-pyrazolidin-3-one (120 mg, 0.49 mmol, 1.00eq) in toluene (20 mL) was slowly added phosphoryl chloride (22.5 mg,1.47 mmol, 3.00 eq). The mixture was then heated at 80° C. for 1 hbefore cooling to room temperature and quenching with H₂O (10 mL). Thevessel was stirred under an atmosphere of N₂ for 8 h before the productwas extracted into EtOAc (200 mL), dried (MgSO₄), and concentrated underreduced pressure. GC/MS proved 88% formation of the desiredintermediate, which was used in subsequent reactions without furtherpurification.

Step 3.4-[1-(4-Trifluoromethoxyphenyl)-4,5-dihydro-1H-pyrazol-3-yl]-benzaldehye:A suspension of3-chloro-1-(4-trifluoromethoxyphenyl)-4,5-dihydro-1H-pyrazole (114 mg,0.43 mmol, 1.00 eq), 4-formylphenylboronic acid (97 mg, 0.65 mmol, 1.50eq), bis(triphenylphosphine)palladium(II) dichloride (10 mg, 0.01 mmol,0.03 eq), 2 M Na₂CO₃ (aq) (0.43 mL, 0.86 mmol, 2.0 eq), and 1,4-dioxane(5 mL) were heated at 150° C. in a microwave reaction vessel for 45 min.The cooled solution was then diluted with EtOAc (20 mL), filtered overCelite®, concentrated to dryness, and purified via chromatography(2:2:1, hexane:EtOAc:acetone) to afford the desired intermediate (50 mg,0.15 mmol, 31%).

Example 10 Preparation of4-[1-(5-bromo-2-chlorophenyl)-1H-imidazol-4-yl]-benzaldehyde

Step 1. 4-[1-(5-Bromo-2-chlorophenyl)-1H-imidazol-4-yl]-benzonitrile.

The compound was prepared according to Liu et al. J. Org. Chem. 2005,70, 10135. 4-(1H-Imidazol-4-yl)-benzonitrile, (75 mg, 0.44 mmol,prepared from 4-(2-bromo-acetyl)-benzonitrile using the method of Lynchet al. J. Am. Chem. Soc. 1994, 116, 11030),4-bromo-1-chloro-2-iodobenzene (169 mg, 0.532 mmol), Cs₂CO₃ (577 mg,1.77 mmol), CuI (3 mg, 0.013 mmol), 8-hydroxyquinoline (2 mg, 0.013mmol), and DMF/H₂O (2 mL 10:1 solution) were combined in a 10 mL CEMMicrowave reaction vessel fitted with magnetic stir bar and subjected tomicrowave irradiation at 150° C. for 30 min. The contents were thenfiltered and concentrated to dryness affording intermediate5-bromo-2-chlorophenyl)-1H-imidazol-4-yl]-benzonitrile (68 mg, 43%).

Step 2. 4-[1-(5-Bromo-2-chlorophenyl)-1H-imidazol-4-yl]-benzaldehyde. Toa suspension of the nitrile (68 mg, 0.19 mmol) in DCM (3 mL) at −78° C.was slowly added diisobutylaluminum hydride (DIBAL) in toluene (0.48 mL,0.475 mmol). The ice bath was then removed and the temperature allowedto warm to between 0 and 10° C. where it was held for 2 h. The contentswere again cooled to −78° C. and slowly made acidic (pH=6) with 1 N HCl(aq). The flask was warmed to ambient temperature overnight beforeremoval of the remaining aluminum salts by filtration. The filtrate wasthen washed with H₂O (5 mL), brine (5 mL), dried (Mg₂SO₄), andconcentrated to dryness affording the intermediate1-(5-bromo-2-chlorophenyl)-1H-imidazol-4-yl]-benzaldehyde (33 mg, 48%).

Example 11 Preparation of4-[5-(4-Propylphenyl)-isoxazol-3-yl]-benzaldehyde

Step 1. 4-(Hydroxyiminomethyl)-benzonitrile. The compound was preparedaccording to Biasotti et al. Bioorg. Med. Chem. 2003, 11, 2247. Asuspension of 4-formylbenzonitrile (500 mg, 3.81 mmol, 1.00 eq),hydroxylamine hydrochloride (290 mg, 4.19 mmol, 1.10 eq), and sodiumacetate (1.56 g, 19.05 mmol, 5.00 eq) in MeOH (50 mL) was heated at 70°C. for 4 h before concentration to dryness. The residue was thenslurried in Et₂O, filtered, and concentrated to afford the desiredintermediate (496 mg, 3.39 mmol, 89%).

Step 2. 4-(Hydroxyimino-bromomethyl)-benzonitrile. The compound wasprepared according to Tanaka et al. Bull. Chem. Soc. Jpn. 1984, 57,2184. A 0.05 M solution of N-bromosuccinimide (724 mg, 4.07 mmol, 1.20eq) in DCM was added dropwise to a 0° C. solution of4-(hydroxyiminomethyl)-benzonitrile (496 mg, 3.39 mmol, 1.00 eq) in DCM(50 mL). The solution was warmed to room temperature before beingvolumetrically partitioned between two different reaction vials. Eachvial was then concentrated and the crude residues were used withoutfurther purification.

Step 3. 4-[5-(4-Propylphenyl)-isoxazol-3-yl]-benzonitrile. A solution of4-(hydroxyimino-bromomethyl)-benzonitrile (381 mg, 1.70 mmol),triethylamine (0.71 mL, 5.10 mmol, 3.0 eq), and1-ethynyl-4-propylbenzene (1.23 g, 8.50 mmol, 5.0 eq) in toluene (20 mL)was heated at 100° C. for 1 h before concentration to dryness andpurification via normal phase chromatography to afford the desiredintermediate (108 mg, 22%). Reduction of the nitrile to thecorresponding aldehyde was accomplished following the DIBAL proceduredescribed earlier.

Example 12 Preparation of4-{1-[4-(1-hydroxypropyl)-phenyl]-1H-pyrazol-3-yl}-benzaldehyde

Step 1. 3-(4-Cyanophenyl)pyrazole. To a round bottom flask equipped withmechanical stir bar and reflux condenser were added p-cyanoacetophenone(5 g, 34.44 mmol) and dimethylformamide dimethylacetal (40 mL). Themixture was stirred at reflux for 5 h before concentration under reducedpressure afforded the crude dimethylamino-acryloylbenzonitrileintermediate. The residue was then suspended in a minimal volume of EtOH(˜20 mL), charged with hydrazine monohydrate (1.67 mL, 34.4 mmol), andheated at 80° C. for 30 min before concentration to yield the crude3-(4-cyanophenyl)pyrazole material (5.59 g, 33 mmol, 96%), of sufficientpurity for use in the subsequent reaction.

Step 2. 4-[1-(4-Propionyl-phenyl)-1H-pyrazol-3-yl]-benzonitrile.4-(1H-Pyrazol-3-yl)-benzonitrile (100 mg, 0.591 mmol),1-(4-bromophenyl)-propan-1-one (126 mg, 0.591 mmol), Cs₂CO₃ (770 mg,2.364 mmol), CuI (4 mg, 0.018 mmol), 8-hydroxyquinoline (3 mg, 0.018mmol), and DMF/H₂O (2 mL 10:1 solution) were combined in a 10 mL CEMMicrowave reaction vessel fitted with magnetic stir bar and subjected tomicrowave irradiation at 150° C. for 30 min. The contents were thenfiltered and concentrated to dryness affording the nitrile (158 mg,0.508 mmol, 86%). Reduction of the nitrile to the corresponding aldehydewas accomplished following the DIBAL procedure described earlier.

Example 13 Preparation of5-(4-formylphenyl)-2-(4-trifluoromethoxy-phenyl)-3,4-dihydro-2H-pyrazole-3,4-dicarboxylicacid diethyl ester

Step 1. Preparation of4-[(4-trifluoromethoxyphenyl)-hydrazonomethyl]-benzaldehyde. Thecompound was prepared according to Paulvannan et al. Tetrahedron. 2000,56, 8071. To a stirred solution of benzene-1,4-dicarbaldehyde (1.50 g,11.2 mmol, 1.0 eq) in i-PrOH (250 mL) was added4-trifluoromethoxy)phenylhydrazine hydrochloride (2.55 g, 11.2 mmol, 1.0eq) portionwise over 5 min. The solution was stirred at ambienttemperature for 1 h before concentration to dryness and purification viachromatography (2:2:1, hexane:EtOAc:acetone) to afford the intermediate(2.48 g, 72%).

Step 2. Chloro-hydrazone synthesis. The intermediate was preparedaccording to Lokanatha Rai and Hassner Synth. Commun. 1989, 19, 2799. Asolution of 4-[(4-trifluoromethoxyphenyl)-hydrazonomethyl]-benzaldehyde(2.48 g, 8.05 mmol, 1.00 eq) and N-chlorosuccinimide (1.61 g, 12.08mmol, 1.5 eq) in i-PrOH (100 mL) was heated at 80° C. for 1 h. Thesolution was then cooled and volumetrically partitioned evenly betweensix different reaction vessels to each contain 1.34 mmol of theintermediate.

Step 3. Pyrazoline synthesis. The compounds were prepared according toPaulvannan et al. Tetrahedron 2000, 56, 8071. To each reaction vesselwere added triethylamine (0.56 mL, 4.02 mmol, 3.00 eq) and therespective acrylates (6.70 mmol, 5.00 eq). The vessels were then heatedat 70° C. for 90 min before concentration to dryness and purificationvia chromatography (2:2:1, hexane:EtOAc:acetone). Reduction of thenitriles to the corresponding aldehydes was accomplished following theDIBAL procedure described earlier.

Example 14 Preparation of4-{1-[4-(2,2,2-trifluoroethoxy)-phenyl]-1H-imidazol-4-yl}-benzaldehyde

4-(2-Bromoacetyl)-benzonitrile (58 mg, 0.21 mmol) and4-(2,2,2-trifluoroethoxy)-phenylamine (50 mg, 0.21 mmol) were combinedin a 100 mL Erlenmeyer flask fitted with magnetic stir bar. The contentswere dissolved in 1 mL of EtOH and stirred at ambient temperature for 2h. The crude intermediate was then transferred to a 100 mL round bottomflask containing KSCN (21 mg, 0.21 mmol) and conc. HCl (18 uL, 0.21mmol). The vessel was heated at 80° C. for 1 h before its contents werepoured into 5 mL of a 1:1 H₂O/NH₄OH solution. The solution was allowedto stand for 24 h, and then the solid was filtered and washed with etherto afford the intermediate imidazolethiol (32 mg, 0.086 mmol, 33%). Anaqueous solution of HNO₃ (1.35 mL, 0.387 mmol) and KNO₃ (1 mg, 0.003mmol) was then added dropwise over 10 min to a suspension of theimidazolethiol in 2 mL of acetic acid. After stirring for 2 h at ambienttemperature the solution was poured into crushed ice and neutralized(pH=7) with 0.1 N NaOH (aq). The intermediate nitrile was isolated byvacuum filtration and dried in a 45° C. vacuum oven for 12 h (23 mg,78%), mp 179° C. Reduction to the corresponding aldehyde wasaccomplished using DIBAL under conditions described previously.

Example 15 Preparation of4-[1-(4-propylphenyl)-1H-imidazol-4-yl]-benzaldehyde

4-Propylaniline (2.70 g, 20 mmol) was added dropwise to a solution of4-cyanophenacyl bromide (2.20 g, 10 mmol) in 5 mL of DMF. This solutionwas then added to 20 mL of a hot (180° C.) formamide solution over 5min, and this solution was allowed to stir at 180° C. for 2 h. Thecooled solution was then poured onto 100 mL of ice, and extracted with2×75 mL of ether. After drying and concentrating, the resulting dark oilwas purified by chromatography (3:1:2 hexanes:EtOAc:DCM). The firstproduct (510 mg) was identified as4-(5-propyl-1H-indol-3-yl)-benzonitrile, mp 140° C. The second fraction(275 mg) was identified as the desired imidazole. ¹H NMR (400 MHz,CDCl₃) δ 7.95 (d, J=6 Hz, 2H), 7.90 (s, 1H), 7.70 (d, J=6 Hz, 2H), 7.68(s, 1H), 7.38 (d, J=4 Hz, 2H), 7.31 (d, J=4 Hz, 2H), 2.69 (t, J=8.9 Hz,2H), 1.68 (m, 2H), 0.98 (t, J=7.5 Hz, 3H); mp 133° C.; ESIMS 288.1(M+H).

Reduction to the corresponding aldehyde was accomplished using DIBALunder conditions described previously. ¹H NMR (300 MHz, CDCl₃) δ 10.02(s, 1H), 8.03 (d, J=6 Hz, 2H), 7.92 (d, J=6 Hz, 2H), 7.90 (s, 1H), 7.72(s, 1H), 7.38 (d, J=4 Hz, 2H), 7.31 (d, J=4 Hz, 2H), 2.69 (t, J=8.9 Hz,2H), 1.68 (m, 2H), 0.98 (t, J=7.5 Hz, 3H); ESIMS 291.1 (M+H); mp 97° C.

Example 16 Preparation of4-[1-(4-trifluoromethoxyphenyl)-1H-imidazol-4-yl]-benzaldehyde

4-Trifluoromethoxyaniline (2.20 g, 12.4 mmol) was added dropwise to asolution of 4-cyanophenacyl bromide (1.50 g, 6.7 mmol) in 5 mL of DMF.This solution was then added to 20 mL of a hot (180° C.) formamidesolution over 5 min, and this solution was allowed to stir at 180° C.for 2 h. The cooled solution was then poured onto 100 mL of ice, andextracted with 2×75 mL of ether. After drying and concentrating, theresulting semi-solid was crystallized from MeOH/H₂O. A secondrecrystallization from MeOH/H₂O removed traces of the formanilideimpurity and furnished 200 mg of pure product, mp 155° C. Anal. Calcd.for C₁₇H₁₀F₃N₃O: C, 62.01; H, 3.06; N, 12.76. Found: C. 61.53; H, 3.13;N, 12.55. Reduction to the corresponding aldehyde was accomplished usingDIBAL under conditions described previously. ¹H NMR (300 MHz, CDCl₃) δ10.0 (s, 1H), 8.05-7.90 (m, 5H), 7.70 (s, 1H), 7.50 (d, J=6 Hz, 2H),7.42 (d, J=6 Hz, 2H); MS 333.0 (M+H); mp 112° C.

Example 17 Preparation of4-[1-(4-trifluoromethoxyphenyl)-1H-imidazol-4-yl]-benzoic acid

A solution of the nitrile (1.1 g, 3.3 mmol) in EtOH (5 mL) and water (2mL) was treated with 1 g of NaOH (20 mmol), and the solution was heatedto reflux for 6 h. It was then cooled and made acidic with 1 N HCl, andthe resulting white solid was filtered and air-dried to give 1.1 g ofthe acid as a light grey solid.

¹H NMR (400 MHz, CDCl₃) δ 11.4 (s, 1H), 7.90 (d, J=6.4 Hz, 2H), 7.89 (s,1H), 7.80 (d, J=8.6 Hz, 2H), 7.63 (d, J=1.3 Hz, 1H), 7.49 (d, J=9.3 Hz,2H), 7.38 (d, J=8.9 Hz, 2H); mp 230° C.

Example 18 Preparation of4-[4-(4-trifluoromethylphenyl)-1H-imidazol-1-yl]-benzaldehyde

4-Trifluoromethylphenyl imidazole (4.0 g, 19 mmol), 4-fluorobenzonitrile(1.2 g, 8.5 mmol) and potassium carbonate (1.5 g, 10.9 mmol) werecombined in 15 mL of DMSO and heated at 100° C. for 6 h. The cooledsolution was then poured onto 100 mL of water and the resulting solidwas filtered and air-dried to give 4.65 g of the imidazole nitrile as awhite solid: mp 252° C.; ¹H NMR (300 MHz, CDCl₃) δ 8.05 (s, 1H), 7.95(d, J=8 Hz, 2H), 7.85 (d, 2H), 7.72 (s, 1H), 7.72 (d, J=8 Hz, 2H), 7.62(d, J=8 Hz, 2H); MS 314.1 (M+H). Anal. Calcd. for C₁₆H₁₀F₃N₃O₂: C,65.18; H, 3.22; N, 13.41. Found: C, 64.49; H, 3.23; N, 13.08. A portionof the nitrile (3.8 g) was reduced in the presence of DIBAL underconditions described previously to give 2.41 g of the correspondingaldehyde. ¹H NMR (300 MHz, CDCl₃) δ 10.1 (s, 1H), 8.10 (d, J=8 Hz, 2H),8.05 (s, 1H), 7.95 (d, J=8 Hz, 2H), 7.75 (s, 1H), 7.7 (m, 4H); MS 317.1(M+H); mp 141° C.

Example 19 Preparation of4-bromo-1-(4-trifluoromethoxyphenyl)-1H-imidazole

A round bottom flask was charged with 4-bromoimidazole (1.15 g, 7.81mmol), CuI (0.07 g, 0.36 mmol), 8-hydroxyquinoline (0.05 g, 0.36 mmol),cesium carbonate (3.39 g, 10.4 mmol) and 4-trifluoromethoxyiodobenzene(1.50 g, 5.21 mmol). A 10:1 mixture of DMF (15 mL) and H₂O (1.5 mL) wereadded to the reaction mixture, and the solution was heated to 130° C.for 4 h. The reaction mixture was then diluted with EtOAc and washedsequentially with water, ammonium chloride (saturated), water and sodiumbicarbonate. The organics were dried over MgSO₄, filtered and purifiedon a reverse phase column to give 820 mg of imidazole as a white solid.MS 308.0 (M+H); mp 139-141° C.

Example 20 Preparation of4-methoxy-2-[1-(4-trifluoromethoxyphenyl)-1H-imidazol-4-yl]-benzaldehyde

4-Bromo-1-(4-trifluoromethoxyphenyl)-1H-imidazole (100 mg, 0.326 mmol),2-formyl-5-methoxyphenylboronic acid (73 mg, 0.41 mmol),bis(triphenylphosphine)palladium dichloride (2 mg, 0.003 mmol), sodiumbicarbonate (49 mg, 0.59 mmol) and 1:1 DME/H₂O (8:8 mL) were combinedand added to a microwave vessel. The reaction mixture was heated in themicrowave with stirring at 100° C. for 12 min. The microwave took 5 minto reach 100° C., then maintained at 100° C. for 12 min, and thencooled. TLC (1:1 EtOAc:cyclohexane) showed the presence of startingmaterials, thus the sample was heated to 100° C. for another 8 min. Uponcooling a precipitate formed; this was filtered and washed with water togive 86 mg of a grey solid. ESIMS 363.0 (M+H).

The following intermediate was also prepared using this procedure:

Example 21 Preparation of2-fluoro-4-[1-(4-trifluoromethoxyphenyl)-1H-imidazol-4-yl]-benzaldehyde

ESIMS 351.0 (M+H).

Example 22 Preparation of1-{4-fluoro-3-[1-(4-trifluoromethoxyphenyl)-1H-imidazol-4-yl]-phenyl}-ethanone

4-Bromo-1-(4-trifluoromethoxyphenyl)-1H-imidazole (200 mg, 0.651 mmol),5-acetyl-2-fluorophenylboronic acid (178 mg, 0.977 mmol),tetrakis(triphenylphosphine)palladium(0) (7 mg, 0.007 mmol), a 2 Naqueous solution of potassium carbonate (0.651 mL) and dioxane (8 mL)were combined and added to a microwave vessel. The reaction mixture washeated in the microwave with stirring to 150° C. for 20 min. LC-MSindicated 88% anticipated product; TLC (1:1 hexanes:EtOAc) indicated thepresence of starting material plus 3 other materials. EtOAc and waterwere added to the reaction mixture. The aqueous layer was extracted withEtOAc and the organic extracts were washed with brine, dried over MgSO₄,and concentrated in vacuo. The crude product was purified bychromatography with gradient elution (100% hexanes to 100% EtOAc)resulting in 90 mg of an off-white solid. ESIMS 265.0 (M+H); mp 129√ C.

Example 23 Preparation of4-[1-(4-trifluoromethoxyphenyl)-1H-[1,2,4]triazol-3-yl]-benzaldehyde

Step 1. 4-(1H-[1,2,4]Triazol-3-yl)-benzonitrile. The general procedureoutlined by Lin et. al. (J. Org. Chem. 1979, 44, 4163) for preparationof 3-(4-nitrophenyl)-1H-[1,2,4]triazole was used. 4-Cyanobenzamide(21.63 g, 0.148 mol) was dissolved in DMF-DMA (100 mL) and was stirredat reflux under N₂ for 8 h. The mixture was concentrated to dryness andsuspended in 50 mL of AcOH. The vessel was then charged with hydrazinemonohydrate (7.18 mL, 0.148 mmol) and stirred at reflux for 1 h beforeconcentration. The desired 4-(1H-[1,2,4]triazol-3-yl)-benzonitrile wasobtained in 98% purity by trituration with Et₂O followed by filtration(12.17 g, 0.072 mol, 48%).

Step 2.4-[1-(4-Trifluoromethoxyphenyl)-1H-[1,2,4]triazol-3-yl]-benzonitrile.The triazole (70 mg, 0.41 mmol), 1-iodo-4-trifluoromethoxybenzene (142mg, 0.493 mmol), Cs₂CO₃ (535 mg, 1.644 mmol), CuI (3 mg, 0.012 mmol),8-hydroxyquinoline (2 mg, 0.012 mmol), and DMF/H₂O (2 mL 10:1 solution)were combined in a 10 mL CEM Microwave reaction vessel fitted withmagnetic stir bar and subjected to microwave irradiation at 150° C. for30 min. The contents were then filtered and concentrated to drynessaffording the 1,3-diphenyl triazole intermediate (18 mg, 13%).

Step 3.4-[1-(4-Trifluoromethoxy-phenyl)-1H-[1,2,4]triazol-3-yl]-benzaldehyde.The nitrile was reduced with DIBAL under conditions previouslydescribed. ¹H NMR (300 MHz, CDCl₃) δ 10.1 (s, 1H), 8.61 (s, 1H), 8.37(d, J=9 Hz, 2H), 8.0 (d, J=8.4 Hz, 2H), 7.8 (d, J=9 Hz, 2H), 7.4 (d,J=8.4 Hz, 2H); ESIMS 334.2 (M+H); mp 137-140° C.

Example 24 Preparation of4-[1-(4-pentafluoroethylsulfanylphenyl)-1H-[1,2,4]triazol-3-yl]-benzaldehyde

Step 1. 1-Bromo-4-pentafluoroethylsulfanylbenzene. The title compoundwas prepared using perfluoroalkylation conditions originally describedby Popov et. al. J. Fluorine Chem. 1982, 21, 365. To a solution of4-bromobenzenethiol (500 mg, 2.64 mmol, 1.00 eq) and triethylbenzylammonium chloride (60 mg, 0.26 mmol, 0.10 eq) in 10 mL of 1:1 Et₂O/NaOH(25% aq) at 0° C. was bubbled 1,1,1,2,2-pentafluoro-2-iodoethane gas for30 min (>5 eq). During this time a UV lamp was directed at the reactionvessel while the temperature was maintained below 10° C. by intermittentuse of an ice bath. The contents were then warmed to room temperature,extracted into Et₂O (300 mL), dried (MgSO₄), and concentrated underreduced pressure. A portion of this crude material was used insubsequent reactions without further purification (200 mg residue: 120mg product, 0.39 mmol, 1.2 eq).

Step 2.4-[1-(4-Pentafluoroethylsulfanylphenyl)-1H-[1,2,4]triazol-3-yl]-benzonitrile.Coupling with 4-(1H-[1,2,4]triazol-3-yl)-benzonitrile as described abovegave4-[1-(4-pentafluoroethylsulfanylphenyl)-1H-[1,2,4]triazol-3-yl]-benzonitrile:70 mg, 46%. Reduction with DIBAL, as described previously, gave thecorresponding aldehyde.

Example 25 Preparation of4-[1-(4-pentafluoroethyloxy-phenyl)-1H-[1,2,4]triazol-3-yl]-benzaldehyde

Step 1. A solution of 3-p-tolyl-1H-[1,2,4]triazole (4.85 g, 30.5 mmol),4-bromophenyl pentafluoroethyl ether (10.0 g, 34.4 mmol), Cs₂CO₃ (25 g,77 mmol), CuI (1.25 g, 6.5 mmol) and 8-hydroxyquinoline (0.35 g, 2.4mmol) in 50 mL of 9:1 DMF/H₂O was stirred vigorously and heated to 130°C. (internal temperature) for 20 h. The solution was then cooled, pouredinto water, and acidified with 2 N HCl to pH 2. Ether (250 mL) was thenadded and the solution was shaken and filtered before separating layers.The organic layer was dried and concentrated, and the resulting gummysolid was heated with 100 mL of hexanes. The hot hexane layer wasdecanted from insoluble residue, the resulting solution cooled to 0° C.and the precipitated solid was filtered and air-dried to furnish 7.0 g(61% based on starting triazole) of1-(4-pentafluoroethyloxy-phenyl)-3-p-tolyl-1H-[1,2,4]triazole as anoff-white solid, mp 130-132° C.; ESIMS 370.8 (M+H).

Step 2. The product from Step 1 (7.0 g, 18.7 mmol) was dissolved in 200mL of acetonitrile and stirred at ambient temperature while cericammonium nitrate (32 g, 58 mmol) in 60 mL of water was added in portionsover 10 min. The solution was then heated to reflux for 4 h, cooled, anddiluted with 200 mL of water. The solution was extracted with 2×200 mLof ether, and the combined organic layer was dried and concentrated togive an orange oil. This material was dissolved in 40 mL of dioxane andtreated with a solution of KOH (5 g, 90 mmol) in 20 mL of water. Thesolution was heated to reflux for 2 h, then cooled and diluted with 100mL of water. The aldehyde precipitated and was collected by filtration.Recrystallization from MeOH/H₂O gave the pure aldehyde as a white solid.¹H NMR (300 MHz, CDCl₃) δ 10.1 (s, 1H), 8.65 (s, 1H), 8.40 (d, J=8.4 Hz,2H), 8.0 (d, J=8.4 Hz, 2H), 7.85 (d, J=9 Hz, 2H), 7.45 (d, J=9 Hz, 2H);ESIMS 384.2 (M+H); mp 137-144° C.

Example 26 Preparation of4-[1-(4-pentafluoroethyloxy-phenyl)-1H-[1,2,4]triazol-3-yl]-benzoic acid

A solution of4-[1-(4-pentafluoroethyloxy-phenyl)-1H-[1,2,4]triazol-3-yl]-benzaldehyde(1.7 g, 4.4 mmol), sodium bromate (2.1 g, 13.9 mmol) and sodiumbisulfate (0.53 g, 4.5 mmol) in 50 mL of acetonitrile was heated toreflux for 5 h, during which time a voluminous precipitate formed. Thesolution was then cooled and poured into 100 mL of water, filtered, anddried to furnish 1.67 g of the acid as a white solid. ¹H NMR (300 MHz,CDCl₃) δ 10.1 (s, 1H), 8.65 (s, 1H), 8.40 (d, J=8.4 Hz, 2H), 8.0 (d,J=8.4 Hz, 2H), 7.85 (d, J=9 Hz, 2H), 7.45 (d, J=9 Hz, 2H); ESIMS 399.2(M+H⁺); mp 225° C.

Example 27 Preparation of4-[1-(4-pentafluoroethyloxy-phenyl)-1H-[1,2,4]triazol-3-yl]-benzoylazide

A solution of4-[1-(4-pentafluoroethyloxy-phenyl)-1H-[1,2,4]triazol-3-yl]-benzoic acid(1.67 g, 4.2 mmol), diphenylphosphoryl azide (1.26 g, 4.58 mmol) andtriethylamine (0.5 g, 5 mmol) in 10 mL of dry t-BuOH was heated to 75°C. for 90 min, resulting in dissolution of the starting acid andsubsequent precipitation of the azide. The cooled solution was thenpoured onto 10 g of ice, and the resulting mixture was filtered anddried to furnish 0.80 g of the azide as a white solid. ¹H NMR (300 MHz,CDCl₃) δ 10.1 (s, 1H), 8.65 (s, 1H), 8.40 (d, J=8.4 Hz, 2H), 8.0 (d,J=8.4 Hz, 2H), 7.85 (d, J=9 Hz, 2H), 7.45 (d, J=9 Hz, 2H); ESIMS 399.2(M+H); mp 175° C. dec.

Example 28 Preparation of4-[1-(4-butyl-phenyl)-1H-[1,2,4]triazol-3-yl]-benzaldehyde

Step 1. 4-[1-(4-Butyl-phenyl)-1H-[1,2,4]triazol-3-yl]-benzonitrile. Asolution of 4-n-butyl phenyl hydrazine (1.0 g, 5 mmol) and4-cyanobenzaldehyde (0.8 g, 6.0 mmol) in 15 mL of i-PrOH was heated on asteam bath for 2 h and then was cooled and diluted with 5 mL of water.The resulting orange solid was filtered and air-dried to give 1.30 g ofthe hydrazone as a yellow solid, mp 107° C. A solution of this hydrazone(1.1 g, 4.0 mmol) and NCS (0.67 g, 5 mmol) in 20 mL of i-PrOH wasstirred under nitrogen at ambient temperature for 2 h, during which timethe original solid dissolved and a new solid formed. The resultingorange solution was then treated with tetrazole (0.45 g, 6.4 mmol) andtriethylamine (960 μL, 7.0 mmol). The orange-brown solution was heatedat reflux for 2 h. The solution was then cooled, diluted with 25 mL ofwater, extracted with EtOAc, dried, concentrated, and purified bychromatography (Biotage, 4:1 Hex:EtOAc) to give 0.42 g (35%) of thetriazole as an off-white solid. ¹H NMR (300 MHz, CDCl₃) δ 8.58 (s, 1H),8.33 (d, J=8 Hz, 2H), 7.78 (d, J=8 Hz, 2H), 7.64 (d, J=8.2 Hz, 2H), 7.33(d, J=8.2 Hz, 2H), 2.70 (t, J=7.8 Hz, 2H), 1.63 (m, 2H), 1.38 (m, 2H),0.95 (t, J=7.5 Hz, 3H); ESIMS 303.1; mp 124° C.

Step 2. 4-[1-(4-Butyl-phenyl)-1H-[1,2,4]triazol-3-yl]-benzaldehyde.Reduction with DIBAL, as described previously, gave the correspondingaldehyde. ¹H NMR (300 MHz, CDCl₃) δ 10.08 (s, 1H), 8.58 (s, 1H), 8.37(d, J=8 Hz, 2H), 7.98 (d, J=8 Hz, 2H), 7.62 (d, J=8.2 Hz, 2H), 7.33 (d,J=8.2 Hz, 2H), 2.70 (t, J=7.8 Hz, 2H), 1.63 (m, 2H), 1.38 (m, 2H), 0.95(t, J=7.5 Hz, 3H); ESIMS 306.1; mp 124° C.

Example 29 Preparation of4-[1-(4-pentafluoroethyl-phenyl)-1H-[1,2,4]triazol-3-yl]-benzaldehyde

Step 1. 1-(4-Pentafluoroethyl-phenyl)-3-p-tolyl-1H-[1,2,4]triazole.Pentafluoroethyl iodide (521 mg, 2.12 mmol) was condensed into a vialcontaining 1-bromo-4-iodobenzene (300 mg, 1.06 mmol), copper(0) powder(135 mg, 2.12 mmol), and DMSO (5 mL). The vial was then sealed andsubjected to microwave irradiation at 150° C. for 60 min. GC/MS provedconsumption of the starting material yielding both1-bromo-4-pentafluoroethylbenzene and 1-iodo-4-pentafluoroethyl-benzeneintermediates. The mixture (1.06 mmol), was transferred to a 250 mLround bottom flask and 3-p-tolyl-1H-[1,2,4]triazole (169 mg, 1.06 mmol),Cs₂CO₃ (1.38 g, 4.24 mmol), CuI (202 mg, 1.06 mmol), 8-hydroxyquinoline(2 mg, 0.011 mmol), and DMF/H₂O (12 mL 10:1 solution) were added and thesolution was refluxed at 160° C. for 6 h. Upon completion, the cooledcontents were poured into H₂O and precipitation was allowed for 1 h. Theprecipitate was collected by vacuum filtration and dried overnight in a45° C. vacuum oven. The crude1-(4-pentafluoroethylphenyl)-3-p-tolyl-1H-[1,2,4]triazole intermediatewas used in step 2 without further purification.

Step 2. Oxidation to the aldehyde. Ammonium cerium(IV) nitrate (3.32 g,4.24 mmol) and the intermediate from Step 1 were combined in a roundbottom flask with acetonitrile and water (20 mL, 1:1). The solution wasstirred at reflux at 110° C. for 4 h, affording a mixture of the3-(4-nitrooxymethyl-phenyl)-1-(4-pentafluoroethyl-phenyl)-1H-[1,2,4]triazoleand4-[1-(4-pentafluoroethyl-phenyl)-1H-[1,2,4]triazol-3-yl]-benzaldehydeintermediates. The acetonitrile was removed under vacuum and the crudeintermediate precipitates were collected by filtration. The material wasthen combined with powdered KOH (178 mg, 3.18 mmol) in dioxane and water(10 mL, 1:1) and was stirred at reflux at 105° C. for 90 min before thedioxane was removed under vacuum allowing precipitation of theintermediate from water. The4-[1-(4-pentafluoroethylphenyl)-1H-[1,2,4]triazol-3-yl]-benzaldehydeintermediate was collected by filtration (35 mg, 0.095 mmol, 9% overallfrom 4-tolyl triazole).

Example 30 Preparation of trifluoromethanesulfonic acid4-[3-(4-formyl-phenyl)-[1,2,4]triazol-1-yl]-phenyl ester

Step 1. 1-(4-Methoxyphenyl)-3-p-tolyl-1H-[1,2,4]triazole was prepared bycoupling 3-p-tolyl-1H-[1,2,4]triazole with 4-iodoanisole underconditions described in Step 1 of the previous example. This materialwas then demethylated using conditions described in Hitchcock et al.Synlett 2006, 2625. Boron tribromide (1 M solution in hexanes; 1.67 mL,1.67 mmol) was added dropwise to a solution of1-(4-methoxyphenyl)-3-p-tolyl-1H-[1,2,4]triazole (300 mg, 1.28 mmol) inDCM (10 mL) at 0° C. under N₂. After addition was complete, the vesselwas warmed to ambient temperature before refluxing at 40° C. for 6 h.The cooled contents were then quenched with H₂O before removal of theDCM and partitioning between EtOAc and water. The organic layer wascollected, washed with brine, dried (MgSO₄), concentrated, and purifiedvia chromatography (3:1:1, hexanes:EtOAc:acetone) to afford the4-(3-p-tolyl-[1,2,4]triazol-1-yl)-phenol intermediate (219 mg, 0.872mmol, 68%). Trifluoromethanesulfonic anhydride (0.16 mL, 0.96 mmol) wasadded dropwise to a solution of the phenol and4-tert-butyl-2,6-dimethylpyridine (142 mg, 0.872 mmol) in DCM (10 mL) at0° C. under N₂. The vessel was warmed to ambient temperature before thesolvent was removed under reduced pressure and the residue purified viachromatography (2:2:1, hexanes:EtOAc:acetone) affording thetrifluoromethanesulfonic acid 4-(3-p-tolyl-[1,2,4]triazol-1-yl)-phenylester intermediate (304 mg, 0.794 mmol, 91%).

Step 2. Oxidation of the 4-methyl intermediate above to thecorresponding aldehyde was carried out using ammonium cerium(IV) nitrateunder conditions described in Step 2 of the previous example.

Example 31 Preparation of4-[5-(4-trifluoromethyl-phenyl)-1H-[1,2,4]triazol-3-yl]-benzaldehyde

Terephthalonitrile (115 mg, 0.90 mmol), 4-trifluoromethylbenzoic acidhydrazide (92 mg, 0.450 mmol), K₂CO₃ (31 mg, 0.225 mmol), and n-butylalcohol (˜2 mL) were combined in a 10 mL CEM Microwave reaction vialfitted with magnetic stir bar and subjected to microwave irradiation at150° C. for 30 min. The contents were then filtered and concentrated todryness. Chromatography (3:1 hexanes/EtOAc) afforded the 1,2,4-triazolenitrile (72 mg, 0.230 mmol, 51%). Reduction with DIBAL then generatedthe corresponding aldehyde.

Example 32 Preparation of4-[1-(3,4-dichloro-phenyl)-5-oxo-4,5-dihydro-1H-[1,2,4]triazol-3-yl]-benzaldehyde

Step 1. 4-Cyanophenyl-oxo-acetic acid. A round bottom flask equippedwith mechanical stirrer and reflux condenser was charged withp-cyanoacetophenone (5 g, 34.44 mol), SeO₂ (9.55 g, 86.1 mmol), andpyridine (˜100 mL). The mixture was stirred at reflux for 6 h beforeprecipitates were removed by filtration and the filtrate was chargedwith 10% HCl (aq) (20 mL). The filtrate was extracted into EtOAc (3×50mL) and the combined organic layers were further extracted into nearlysaturated NaHCO₃. The aqueous layer was then carefully made acidic(pH=1) with conc. HCl affording a small crop of the desired product. Theremainder of the oxo acetic acid was obtained by extracting into EtOAc,drying (MgSO₄), and concentration (1.69 g, 28%).

Step 2.4-[1-(3,4-Dichloro-phenyl)-5-oxo-4,5-dihydro-1H-[1,2,4]triazol-3-yl]-benzonitrile.A suspension of 4-cyanophenyl-oxo-acetic acid (100 mg, 0.571 mmol),(3,4-dichlorophenyl)hydrazine hydrochloride (122 mg, 0.571 mmol), 12.1 NHCl (5 uL, 0.057 mmol), and H₂O (˜10 mL) in a 25 mL reaction vial wasstirred vigorously at ambient temperature for 24 h. The hydrazone wasobtained by vacuum filtration and placed into a 100 mL round bottomflask with a magnetic stir bar. The flask was then supplemented withtriethylamine (0.08 mL, 0.571 mmol), diphenylphosphoryl azide (157 mg,0.571 mmol), and toluene (20 mL) before heating at 110° C. for 1 h. Uponcooling the contents were quenched with 10% NaOH (aq) and made acidic(pH 1) with conc. HCl. Precipitation was allowed for 15 min before theintermediate was obtained by vacuum filtration and dried overnight in a45° C. vacuum oven (16 mg, 8%). The nitrile was reduced to the aldehydeusing DIBAL under conditions previously described.

Example 33 Preparation of4-[1-(4-Chloro-phenyl)-1H-[1,2,3]triazol-4-yl]-benzaldehyde

Following the procedure published by Feldman et al. (Org. Lett. 2004, 6,3897), a suspension of 4-ethynylbenzonitrile (50 mg, 0.393 mmol),1-chloro-4-iodobenzene (94 mg, 0.393 mmol), L-proline (9 mg, 0.079mmol), ascorbic acid (7 mg, 0.039 mmol), NaN₃ (31 mg, 0.472 mmol), CuSO₄(3 mg, 0.020 mmol), and Na₂SO₄ (11 mg, 0.079 mmol) in DMSO (1.5 mL) washeated at 65° C. for 24 h. Upon cooling the mixture was diluted with H₂Oand stirred for 30 min at ambient temperature. The intermediate4-[1-(4-chloro-phenyl)-1H[1,2,3]triazol-4-yl]-benzonitrile (54 mg, 48%)was then obtained by vacuum filtration after washing with copiousvolumes of H₂O and 20% NH₄OH (˜20 mL). Reduction to the aldehyde wasthen conducted under conditions previously described.

Example 34 Preparation of4-[5-(4-trifluoromethyl-phenyl)-tetrazol-2-yl]-benzaldehyde

This aldehyde was prepared from 4-trifluoromethylbenzaldehyde byfollowing the route described in Roppe et al. J. Med. Chem. 2004, 47,4645.

Example 35 Preparation of4-[5-(4-trifluoromethoxy-phenyl)-pyridin-3-yl]-benzaldehyde

Step 1. 3,5-Dibromopyridine (4.4 mmol), 4-trifluoromethoxyphenyl boronicacid (5.1 mmol), tetrakis(triphenylphosphine)palladium(0) (0.04 mmol), 2M potassium carbonate (8.44 mmol) and dioxane (21 mL) were combined in avial and heated by microwave for 10 min at 150° C. The reaction mixturewas taken up in ether and washed with brine. The ether layer was driedover magnesium sulfate, was filtered and the solvent removed in vacuo.The crude mixture was purified by silica gel chromatography to yield 130mg of 3-bromo-5-(4-trifluoromethoxy-phenyl)-pyridine as a yellow solid.¹H NMR (400 MHz, CDCl₃) δ 8.71 (m, 2H), 8.00 (t, J=2.1 Hz, 1H), 7.58 (d,J=8.8 Hz, 2H), 7.34 (d, J=8.0 Hz, 2H); EIMS 317 m/z (M⁺).

Step 2. The compound was prepared by palladium-catalyzed arylation ofthe product of step 1 with 4-formylphenyl boronic acid.

Example 36 Preparation of4-[4-(4-trifluoromethoxyphenyl)-pyridin-2-yl]-benzaldehyde

Step 1. The compound was prepared by palladium-catalyzed arylation of2-chloro-4-iodopyridine with 4-trifluoromethoxyphenyl boronic acid.

Step 2. 2-Chloro-4-(4-trifluoromethoxyphenyl)-pyridine (0.55 mmol)starting from 2-chloro-4-iodopyridine, 4-formylphenyl boronic acid (0.82mmol), tetrakis(triphenylphosphine)palladium(0) (0.005 mmol), 2 Mpotassium carbonate (0.55 mL) and dioxane (3 mL) were combined in a vialand irradiated by microwave for 15 min at 150° C. The reaction mixturewas taken up in EtOAc and washed with brine. The organic layer was driedover magnesium sulfate, was filtered and the solvent removed in vacuo.Purification by silica gel chromatography (EtOAc/hexanes) yielded 120 mgof an off-white solid. ¹H NMR (400 MHz, CDCl₃) δ 10.11 (s, 1H), 8.81 (d,J=4.8 Hz, 1H), 8.24 (d, J=8.7 Hz, 2H), 8.03 (d, J=8.4 Hz, 2H), 7.96 (m,1H), 7.73 (d, J=9.0 Hz, 2H), 7.49 (dd, J=5.3, 1.8 Hz, 1H), 7.37 (d,J=8.1 Hz, 2H); EIMS 343 m/z (M⁺).

Example 37 Preparation of4-[6-(4-trifluoromethoxy-phenyl)-pyridin-2-yl]-benzaldehyde

Step 1. 4-(6-Bromopyridin-2-yl)-benzaldehyde (0.31 mmol) was prepared asin Puglisi et al. Eur. J. Org. Chem. 2003, 8, 1552-1558.

Step 2. 4-[6-(4-Trifluoromethoxyphenyl)-pyridin-2-yl]-benzaldehyde.4-(6-Bromo-pyridin-2-yl)-benzaldehyde (0.31 mmol), 4-trifluoromethoxyboronic acid (0.46 mmol), tetrakis(triphenylphosphine)palladium(0)(0.003 mmol), 2 M potassium carbonate (0.31 mL) and dioxane (2 mL) werecombined in a vial and irradiated by microwave for 10 min at 150° C. Thereaction mixture was taken up in ether and washed with brine. Theorganic layer was dried over magnesium sulfate, was filtered and thesolvent removed in vacuo. Purification by silica gel chromatography(EtOAc/hexanes) yielded 80 mg of the product as an off-white solid. ¹HNMR (400 MHz, CDCl₃) δ 10.11 (s, 1H), 8.32 (d, J=8.5 Hz, 2H), 8.19 (d,J=8.1 Hz, 2H), 8.03 (d, J=8.4 Hz, 2H), 7.89 (t, J=7.9 Hz, 1H), 7.79 (d,J=7.7 Hz, 1H), 7.74 (d, J=8.0 Hz, 1H), 7.35 (d, J=8.3 Hz, 2H); EIMS 343m/z (M⁺); mp 109-112° C.

Example 38 Preparation of4-[6-(4-trifluoromethoxyphenyl)-pyrimidin-4-yl]-benzaldehyde

Step 1. 4-Chloro-6-(4-trifluoromethoxy-phenyl)-pyrimidine was preparedby palladium-catalyzed arylation of 4,6-dichloropyrimidine and4-trifluoromethoxyphenyl boronic acid. ¹H NMR (400 MHz, CDCl₃) δ 9.05(s, 1H), 8.14 (d, J=9.8 Hz, 2H), 7.74 (m, 1H), 7.36 (d, J=8.4 Hz, 2H);EIMS 274 m/z (M⁺).

Step 2. The compound was prepared by palladium-catalyzed arylation ofthe product of step 1 with 4-formylphenyl boronic acid. ¹H NMR (400 MHz,CDCl₃) δ 10.15 (s, 1H), 9.38 (d, J=0.9 Hz, 1H), 8.33 (d, J=8.4 Hz, 2H),8.23 (d, J=8.5 Hz, 2H), 8.16 (d, J=0.8 Hz, 1H), 8.08 (d, J=8.8 Hz, 2H),7.40 (d, J=8.1 Hz, 2H); EIMS 344 m/z (M⁺).

Example 39 Preparation of4-[2-(4-trifluoromethoxyphenyl)-pyrimidin-4-yl]-benzaldehyde

Step 1. 4-Chloro-2-(4-trifluoromethoxyphenyl)-pyrimidine. The titlecompound was prepared by palladium-catalyzed arylation of2,4-dichloropyrimidine and 4-trifluoromethoxyphenyl boronic acid. ¹H NMR(400 MHz, CDCl₃) δ 8.68 (d, J=5.6 Hz, 1H), 8.16 (d, J=9.1 Hz, 2H), 7.65(d, J=5.3 Hz, 1H), 7.36 (dd, J=9.2, 0.9 Hz, 2H); EIMS 274 m/z (M⁺); mp70-73° C.

Step 2. The compound was prepared by palladium-catalyzed arylation ofthe product of step 1 with 4-formylphenyl boronic acid. ¹H NMR (400 MHz,CDCl₃) δ 10.13 (s, 1H), 8.91 (d, J=4.8 Hz, 1H), 8.74 (d, J=8.5 Hz, 2H),8.28 (d, J=8.4 Hz, 2H), 8.03 (d, J=8.4 Hz, 2H), 7.65 (d, J=5.3 Hz, 1H),7.39 (d, J=8.6 Hz, 2H); EIMS 344 m/z (M⁺).

Example 40 Preparation of4-[4-(4-trifluoromethoxyphenyl)-pyrimidin-2-yl]-benzaldehyde

Step 1. 4-(4-Chloropyrimidin-2-yl)-benzaldehyde. The compound wasprepared by palladium-catalyzed arylation of 2,4-dichloropyrimidine and4-formylphenyl boronic acid. ¹H NMR (400 MHz, CDCl₃) δ 10.13 (s, 1H),8.74 (d, J=5.0 Hz, 1H), 8.27 (d, J=7.8 Hz, 2H), 8.04 (d, J=7.9 Hz, 2H),7.74 (m, 1H); EIMS 218 m/z (M⁺).

Step 2. The compound was prepared by palladium-catalyzed arylation ofthe product of Step 1 with 4-trifluoromethoxyphenyl boronic acid. ¹H NMR(400 MHz, CDCl₃) δ 10.14 (s, 1H), 8.91 (d, J=4.2 Hz, 1H), 8.63 (d, J=8.5Hz, 2H), 8.37 (d, J=8.4 Hz, 2H), 8.06 (d, J=8.8 Hz, 2H), 7.67 (d, J=5.4Hz, 1H), 7.35 (d, J=8.7 Hz, 2H); EIMS 344 m/z (M⁺).

Example 41 Preparation of4-[6-(4-trifluoromethoxyphenyl)-pyrazin-2-yl]-benzaldehyde

Step 1. 2-Chloro-6-(4-trifluoromethoxyphenyl)-pyrazine. The compound wasprepared by palladium-catalyzed arylation of 2,6-dichloropyrazine and4-trifluoromethoxyphenyl boronic acid. ¹H NMR (400 MHz, CDCl₃) δ 8.94(s, 1H), 8.57 (s, 1H), 8.10 (d, J=9.0 Hz, 2H), 7.37 (d, J=8.4 Hz, 2H);EIMS 274 m/z (M⁺); mp 58-60° C.

Step 2. The compound was prepared by palladium-catalyzed arylation ofthe product of step 1 with 4-formylphenyl boronic acid. ¹H NMR (400 MHz,CDCl₃) δ 10.13 (s, 1H), 9.07 (s, 1H), 9.03 (s, 1H), 8.33 (d, J=8.1 Hz,2H), 8.21 (d, J=8.7 Hz, 2H), 8.07 (d, J=7.6 Hz, 2H), 7.40 (d, J=8.3 Hz,2H); EIMS 344 m/z (M⁺).

Example 42 Preparation of4-[2-(4-trifluoromethoxyphenyl)-pyrimidin-5-yl]-benzaldehyde

Step 1. 4-(2-Chloropyrimidin-5-yl)-benzaldehyde. The compound wasprepared by palladium-catalyzed arylation of 2,5-dichloropyrimidine and4-formylphenyl boronic acid.

Step 2. 4-(2-Chloropyrimidin-5-yl)-benzaldehyde (0.92 mmol),4-trifluoromethoxyphenyl boronic acid (1.10 mmol),dichlorobis(triphenylphosphine)palladium(II) (0.01 mmol), 2 M potassiumcarbonate (0.92 mL) and dioxane (5 mL) were combined in a vial andirradiated by microwave for 10 min at 150° C. The organic layer from thereaction mixture was loaded directly onto silica and dried in vacuo.Purification by silica gel chromatography (EtOAc/hexanes) yielded 140 mgof a white solid. ¹H NMR (400 MHz, CDCl₃) δ 10.11 (s, 1H), 9.07 (s, 2H),8.57 (d, J=9.0 Hz, 2H), 8.07 (d, J=8.5 Hz, 2H), 7.82 (d, J=8.3 Hz, 2H),7.35 (d, J=8.3 Hz, 2H); EIMS 344 m/z (M⁺).

Example 43 Preparation of4-[5-(4-trifluoromethoxyphenyl)-pyrimidin-2-yl]-benzaldehyde

Step 1. 2-Chloro-5-(4-trifluoromethoxyphenyl)-pyrimidine. The compoundwas prepared by palladium-catalyzed arylation of 2,5-dichloropyrimidinewith 4-trifluoromethoxyphenyl boronic acid.

Step 2. 2-Chloro-5-(4-trifluoromethoxyphenyl)-pyrimidine (4.22 mmol),4-formylphenyl boronic acid (5.1 mmol),dichlorobis(triphenylphosphine)palladium(II) (0.05 mmol), 2 M potassiumcarbonate (4.2 mL) and dioxane (21 mL) were combined in a vial andirradiated by microwave for 20 min at 150° C. The organic layer from thereaction mixture was loaded directly onto silica and dried in vacuo.Purification by silica gel chromatography (EtOAc/hexanes) yielded 75 mgof a white solid. ¹H NMR (400 MHz, CDCl₃) δ 10.13 (s, 1H), 9.06 (s, 2H),8.68 (d, J=8.8 Hz, 2H), 8.03 (d, J=8.3 Hz, 2H), 7.68 (d, J=8.8 Hz, 2H),7.40 (d, J=8.7 Hz, 2H); EIMS 344 m/z (M⁺).

Example 44 Preparation of4-heptafluoropropyl-6-(4-nitro-phenyl)-2-(4-trifluoromethyl-phenyl)-pyrimidine

Step 1.4-Heptafluoropropyl-6-(4-nitrophenyl)-2-(4-trifluoromethyl-phenyl)-pyrimidine.A solution of4-heptafluoropropyl-2-methylsulfanyl-6-(4-nitrophenyl)-pyrimidine (1.20g, 2.90 mmol, prepared from1-(4-nitrophenyl-4,4,5,5,6,6,6-heptafluorohexane-1,3-dione according toGreen et al. WO 200138311 A2), 4-trifluoromethylphenylboronic acid(0.608 g, 3.2 mmol), trifurylphosphine (114 mg, 0.49 mmol), and copper(II) 2-thiophenecarboxylate (750 mg, 3.9 mmol) were combined in 15 mL ofdry THF and heated to 50° C. The catalysttris(dibenzylideneacetone)dipalladium(0)-chloroform adduct (60 mg, cat)was then added in three portions over 3 h, and the solution was thenallowed to stir at 50° C. overnight. Concentration and chromatography(Biotage, 5:1 hexane/DCM) furnished 0.60 g (40%) of the title compoundas a light yellow solid. EIMS 514.0 (M+H); mp 191° C.

Step 2.4-Heptafluoropropyl-6-(4-aminophenyl)-2-(4-trifluoromethyl-phenyl)-pyrimidine.A solution of4-heptafluoropropyl-2-(4-trifluoromethylphenyl)-6-(4-nitrophenyl)-pyrimidine(0.18 g, 0.35 mmol), iron powder (0.20 g, 3.5 mmol), ferric ammoniumsulfate (0.15 g, 0.3 mmol) in 3:1 EtOH/water was heated on a steam bathfor 3 h. Then it was cooled, diluted with 50 mL of Et₂O, filteredthrough Celite®, and concentrated to give the aniline as a yellow solid.¹H NMR (300 MHz, CDCl₃) δ 8.75 (d, J=8 Hz, 2H), 8.18 (d, J=8 Hz, 2H),7.90 (s, 1H), 7.80 (d, J=8 Hz, 2H), 6.82 (d, J=8 Hz, 2H), 4.20 (s, 2H).

Example 45 Preparation of4-trifluoromethyl-6-(4-aminophenyl)-2-(4-trifluoromethyl-phenyl)-pyrimidine

Step 1.4-Trifluoromethyl-6-(4-nitrophenyl)-2-(4-trifluoromethyl-phenyl)-pyrimidine.A solution of4-trifluoromethyl-2-methylsulfanyl-6-(4-nitrophenyl)-pyrimidine (1.25 g,4.0 mmol, prepared from 1-(4-nitrophenyl-4,4,4-trifluorobutane-1,3-dioneaccording to Green et al. WO 200138311 A2),4-trifluoromethylphenylboronic acid (0.95 g, 5.0 mmol),trifurylphosphine (140 mg, 0.60 mmol), and copper (II)2-thiophenecarboxylate (1.05 g, 5.0 mmol) were combined in 25 mL of dryTHF and heated to 52° C. The catalysttris(dibenzyl-ideneacetone)dipalladium(0)-chloroform adduct (100 mg) wasthen added in three portions over 3 h, and the solution was then allowedto stir at 50° C. for 12 h. Concentration and chromatography (Biotage,4:1 hexane/DCM) furnished 0.67 g (41%) of the title compound as a lightyellow solid. ¹H NMR (300 MHz, CDCl₃) δ 8.75 (d, J=8 Hz, 2H), 8.41 (s,4H), 8.03 (s, 1H), 7.80 (d, J=8 Hz, 2H); EIMS 414.1 (M+H); mp 162° C.

Step 2.4-Trifluoromethyl-6-(4-aminophenyl)-2-(4-trifluoromethyl-phenyl)-pyrimidine.A solution of4-trifluoromethyl-2-(4-trifluoromethylphenyl)-6-(4-nitrophenyl)-pyrimidine(0.50 g, 1.2 mmol), iron powder (0.50 g, 9 mmol), ferric ammoniumsulfate (0.5 g, 1.0 mmol) in 30 mL of 3:1 EtOH-water was heated on asteam bath for 3 h. Then it was cooled, diluted with 50 mL of diethylether, filtered through Celite®, and concentrated. The crude amine waspurified by Biotage column (4:1:1 Hexanes/EtOAc/DCM) to give 0.22 g ofpure aniline. This material was used directly in the formation of thecorresponding carbamate. ¹H NMR (300 MHz, CDCl₃) δ 8.75 (d, J=8 Hz, 2H),8.16 (d, J=8 Hz, 2H), 7.81 (s, 1H), 7.77 (d, J=8 Hz, 2H), 6.82 (d, J=8Hz, 2H), 4.15 (s, 2H).

Example 46 Preparation of4-[2-(4-trifluoromethyl-phenyl)-pyrimidin-4-yl]-phenylamine

Step 1. 4-(4-Nitrophenyl)-2-(4-trifluoromethyl-phenyl)-pyrimidine. To82.7 mg (3.60 mmol) of sodium metal dissolved in 3 mL of absolute EtOHwas added 938 mg (3.60 mmol) of 4-trifluoromethylbenzamidinehydrochloride dihydrate followed by 4 mL of EtOH. After 30 min, 498 mg(2.26 mmol) of 3-dimethylamino-1-(4-nitrophenyl)-propenone was added andthe mixture was heated at reflux approximately 66 h and was allowed tocool. The mixture was concentrated to a tan solid which was trituratedunder saturated sodium bicarbonate. The solid was collected and airdried to give 937 mg. It was then dissolved in chloroform/EtOAc and waspassed over silica gel eluting with 7:3 chloroform/EtOAc to afford 710mg (91%) of the title compound. ¹H NMR ε 9.01 (d, J=5.3 Hz, 1H), 8.73(d, J=8.2 Hz, 2H), 8.43 (s, 4H), 7.82 (d, J=8.1 Hz, 2H), 7.76 (d, J=5.2Hz, 1H); EIMS 345 (M⁺, 100), 299 (57); mp 175-176.5° C.

Anal. Calcd. for C₁₇H₁₀F₃N₃O₂: C, 59.13; H, 2.92; N, 12.17. Found: C,58.82; H, 2.63; N, 11.98.

Step 2. 4-[2-(4-Trifluoromethyl-phenyl)-pyrimidin-4-yl]-phenylamine. Amixture of 670 mg (1.94 mmol) of the nitrobenzene4-(4-nitrophenyl)-2-(4-trifluoromethyl-phenyl)-pyrimidine and 75 mg of10% Pd/C in 30 mL of EtOH was placed on a Parr shaker at 40 psi hydrogengas at room temperature. After 7 h the mixture was filtered throughCelite® and the EtOH was removed in vacuo. The residue was partitionedbetween EtOAc and saturated sodium bicarbonate, and the organic phasewas dried (MgSO₄). Concentration gave a solid which was dissolved inEtOAc and was filtered through a plug of silica gel. Concentration gave500 mg (82%) of the titled compound. ¹H NMR δ 8.75 (d, J=5.30 Hz, 1H),8.67 (d, J=8.3 Hz, 2H), 8.10 (d, J=8.9 Hz, 2H), 7.75 (d, J=7.9 Hz, 2H),7.54 (d, J=5.3 Hz, 1H), 6.80 (d, J=8.6 Hz, 2H), 4.03 (br s, 2H); MS(API-ES+) 316 ([M+H]⁺, 100); mp 166-167° C. Anal. Calcd. for C₁₇H₁₂F₃N₃:C, 64.76; H, 3.84; N, 13.33. Found: C, 64.37; H, 3.71; N, 13.08.

Example 47 Preparation of2-chloro-4-[3-(4-trifluoromethyl-phenyl)-[1,2,4]triazol-1-yl]-phenylamine

Step 1.1-(3-Chloro-4-nitrophenyl)-3-(4-trifluoromethyl-phenyl)-1H-[1,2,4]triazole.A solution of NBS (180 mg, 1 mmol) in 4 mL of CH₂Cl₂ was stirred undernitrogen at 0° C. while dimethyl sulfide (110 mg, 1.8 mmol) was addedvia syringe. The solution, which forms a white solid, was then cooled to−20° C., and(N-(3-chloro-4-nitrophenyl)-N′-(4-trifluoromethyl-benzylidene)-hydrazine(200 mg, 0.58 mmol) in 4 mL of DCM was added. The solution was allowedto warm to ambient temperature and stirred for an additional 2 h. Theresulting orange solution was then diluted with 25 mL of DCM and washedwith water and brine before drying and concentrating. The resultingorange solid hydrazonyl bromide (150 mg) was then treated directly withtetrazole (25 mg, 0.35 mmol) and triethylamine (50 μL, 0.35 mmol) in 5mL of absolute EtOH. The resulting orange-brown solution was heated atreflux for 2 h. TLC shows that the initial bromide was first convertedinto two yellow intermediates, which then disappeared and were replacedby a single, colorless, spot. The orange solution was then diluted with10 mL of water, yielding a tan-yellow solid which was filtered,air-dried, and recrystallized from toluene to give 60 mg of a yellow-tansolid. ¹H NMR (300 MHz, CDCl₃) δ 8.60 (s, 1H), 8.41 (d, J=8.7 Hz, 1H),8.33 (d, J=7.5 Hz, 2H), 7.90 (d, J=2 Hz, 1H), 7.70 (d, J=7.5 Hz, 2H),7.65 (dd, J=8.7, 2 Hz, 1H); EIMS 368.9; mp 185° C. Anal. Calcd. forC₁₅H₈ClF₃N₄O₂: C, 48.86; H, 2.19; N, 15.20. Found: C, 48.39; H, 2.61; N,14.91.

Step 2.2-Chloro-4-[3-(4-trifluoromethyl-phenyl)-[1,2,4]triazol-1-yl]-phenylamine.A solution of the nitrophenyl derivative (0.75 g, 2.0 mmol) in 7 mL ofMeOH and 3 mL of water was treated with iron powder (0.7 g, 12.5 mmol)and ferrous ammonium sulfate (hexahydrate; 0.7 g, 1.8 mmol). Thesolution was heated on a steam bath for 3 h, whereupon TLC showedcomplete conversion to a more polar, fluorescent product. The solutionwas cooled and filtered, and the filtrate was concentrated in vacuo andpurified by chromatography through a short plug of silica gel (7:2:1hexane/EtOAc/DCM) to give 0.55 g of the amine as a light tan solid. ¹HNMR (300 MHz, CDCl₃) δ 8.40 (s, 1H), 8.31 (d, J=8.4 Hz, 1H), 7.72 (d,J=8.4 Hz, 2H), 7.69 (d, J=2 Hz, 1H), 7.42 (dd, J=8.5, 2 Hz, 1H), 6.9 (d,J=8.4 Hz, 1H); EIMS 340.4, 342.3 (M+H); mp 148° C. Anal. Calcd. forC₁₅H₁₀ClF₃N₄: C, 53.19; H, 2.98; N, 16.83. Found: C, 52.90H, 3.10; N,16.83.

Example 48 Preparation of4-[1-(4-Trifluoromethoxyphenyl)-1H-[1,2,4]triazol-3-yl]-phenylamine

Step 1.1-(4-Trifluoromethoxyphenyl)-3-(4-nitrophenyl)-1H-[1,2,4]triazole. Asolution of NBS (0.70 g, 3.9 mmol) in 25 mL of CH₂Cl₂ was stirred undernitrogen at 0° C. while dimethyl sulfide (0.40 g, 6.5 mmol) was addedvia syringe. The solution, which forms a white solid, was then cooled to−20° C., andN-(4-nitrobenzylidene)-N′-(4-trifluoromethoxyphenyl)-hydrazine (0.70 g,2.15 mmol) in 10 mL of DCM was added. The solution was allowed to warmto ambient temperature and stirred an additional 2 h. The resultingorange solution was then diluted with 25 mL of DCM and washed with waterand brine before drying and concentrating. The resulting orange solidhydrazonyl bromide (0.9 g) was then treated directly with tetrazole (154mg, 2.2 mmol) and triethylamine (280 μL, 0.23 mmol) in 5 mL of absoluteEtOH. The resulting orange-brown solution was heated at reflux for 2 h.TLC showed that the initial bromide was first converted into two yellowintermediates, which were replaced by a single, colorless, spot. Theorange solution was then concentrated and purified by chromatography(2:1:2 Hexane/EtOAc/DCM), yielding 0.30 g of the title compound as alight yellow solid. ¹H NMR (300 MHz, CDCl₃) δ 8.68 (s, 1H), 8.40 (d, J=5Hz, 2H), 8.35 (d, J=5 Hz, 2H), 7.85 (d, J=8 Hz, 2H), 7.42 (d, J=8 Hz,2H); EIMS 350 (M⁺, 100), 299 (57); mp 147° C.

Step 2.4-[1-(4-Trifluoromethoxyphenyl)-1H-[1,2,4]triazol-3-yl]-phenylamine.Catalytic reduction using a Pd/C catalyst in EtOH under hydrogenatmosphere gave the corresponding aniline as a light grey solid. ¹H NMR(300 MHz, CDCl₃) δ 8.50 (s, 1H), 8.00 (d, J=8.4 Hz, 2H), 7.78 (d, J=8.7Hz, 2H), 7.35 (d, J=8 Hz, 2H), 6.76 (d, J=8.7 Hz, 2H), 3.9 (br s, 2H);EIMS 321; mp 160° C.

Example 49 Preparation of4-[1-(4-Pentafluoroethyloxyphenyl)-1H-[1,2,4]triazol-3-yl]-phenylamine

Step 1.1-(4-Pentafluoroethyloxyphenyl)-3-(4-nitrophenyl)-1H-[1,2,4]triazole. Aslurry of 3-(4-nitrophenyl) triazole (11.4 g, 60 mmol),1-iodo-4-pentafluoroethoxybenzene (20 g, 60 mmol), cesium carbonate(39.0 g, 120 mmol), CuI (3.5 g, 18 mmol), 8-hydroxyquinoline (2.0 g,13.8 mmol) and 155 mL of 9:1 DMF-H₂O were heated at 150° C. for 5 h,then cooled and the contents poured onto 150 mL of water and extractedwith 2×100 mL of Et₂O. The organic layer was dried and concentrated, andthe solid residue recrystallized from MeOH and water to give 11.8 g(49%) of the nitrotriazole as a tan solid. ¹H NMR (300 MHz, CDCl₃) δ8.68 (s, 1H), 8.40 (d, J=5 Hz, 2H), 8.35 (d, J=5 Hz, 2H), 7.85 (d, J=8Hz, 2H), 7.42 (d, J=5.2 Hz, 8 Hz, 2H); EIMS 400 (M⁺); mp 170-175° C.

Step 2.4-[1-(4-Pentafluoroethyloxyphenyl)-1H-[1,2,4]triazol-3-yl]-phenylamine.Catalytic reduction using a Pd/C catalyst in EtOH under hydrogenatmosphere gave the corresponding aniline as a light tan solid. ¹H NMR(300 MHz, CDCl₃) δ 8.55 (s, 1H), 8.00 (d, J=7 Hz, 2H), 7.78 (d, J=8 Hz,2H), 7.35 (d, J=8 Hz, 2H), 6.78 (d, J=8 Hz, 2H), 3.9 (br s, 2H); EIMS371; mp 160° C.

Example 50 Preparation of4-[1-(4-heptafluoropropyloxyphenyl)-1H-[1,2,4]triazol-3-yl]-phenylamine

Step 1.1-(4-Heptafluoropropyloxyphenyl)-3-(4-nitrophenyl)-1H-[1,2,4]triazole. Aslurry of 3-(4-nitrophenyl) triazole (1.0 g, 5.2 mmol),1-iodo-4-heptafluoropropyloxybenzene (6.1 g, 15.8 mmol), cesiumcarbonate (10.0 g, 30.7 mmol), CuI (900 mg, 4.7 mmol), and8-hydroxyquinoline (500 mg, 3.4 mmol) in 40 mL of 9:1 DMF-H₂O was heatedat 150° C. for 12 h, then cooled and the contents poured onto 50 mL ofwater and 50 mL of concentrated NH₄OH. The blue solution was extractedwith 100 mL of ether and the organic layer was separated and filtered toremove some insoluble material, then dried and concentrated. The solidresidue was recrystallized from MeOH/water to furnish 4.69 g of thenitrophenyl triazole as a light tan solid. ¹H NMR (300 MHz, CDCl₃) δ8.66 (s, 1H), 8.40 (m, 4H), 7.85 (d, J=8 Hz, 2H), 7.42 (d, J=8 Hz, 2H);EIMS 450.1 (M⁺); mp 114-116° C.

Step 2.4-[1-(4-Heptafluoropropyloxyphenyl)-1H-[1,2,4]triazol-3-yl]-phenylamine.Catalytic reduction under the conditions described above gave thecorresponding aniline as a light tan solid. ¹H NMR (300 MHz, CDCl₃) δ8.54 (s, 1H), 8.00 (d, J=8 Hz, 2H), 7.80 (d, J=8 Hz, 2H), 7.40 (d, J=8Hz, 2H), 6.78 (d, J=8 Hz, 2H), 3.9 (br s, 2H); EIMS 421.3 (M+1); mp181-183° C.

Example 51 Preparation of4-[4-(4-trifluoromethylphenyl)-imidazol-1-yl]-phenylamine

Step 1. 4-[4-(4-Trifluoromethylphenyl)-1H-imidazol-1-yl]-nitrobenzene.4-Trifluoromethylphenyl imidazole (1.43 g, 6.7 mmol), 4-fluoronitrobenzene (1.2 g, 8.5 mmol) and potassium carbonate (1.5 g, 10.9mmol) were combined in 15 mL of DMF and heated at 100° C. for 6 h. Thecooled solution was then poured onto 100 mL of water and the resultingsolid was filtered and air-dried to give 1.0 g of the title imidazole asa light yellow solid, mp 197° C. Anal. Calcd. for C₁₆H₁₀F₃N₃O₂: C,57.66; H, 3.02; N, 12.61. Found: C, 57.69; H, 3.01; N, 12.48.

Step 2. 4-[4-(4-Trifluoromethylphenyl)-imidazol-1-yl]-phenylamine.Catalytic reduction using a Pd/C catalyst in EtOH under hydrogenatmosphere gave the corresponding aniline as a light grey solid. ¹H NMR(400 MHz, CDCl₃) δ 7.90 (d, J=7 Hz, 2H), 7.75 (s, 1H), 7.65 (d, J=7 Hz,2H), 7.52 (s, 1H), 7.19 (d, J=8 Hz, 2H), 6.75 (d, J=8 Hz, 2H), 3.8 (brs, 2H); EIMS 302.0; mp 142-143° C.

Example 52 Preparation of4-[1-(4-trifluoromethylphenyl)-1H-imidazol-4-yl]-phenylamine

Step 1. 4-[4-(4-Trifluoromethylphenyl)-1H-imidazol-1-yl]-nitrobenzene.Prepared as in step 1 of the preceding example.

Step 2. 4-[1-(4-Trifluoromethylphenyl)-1H-imidazol-4-yl]-phenylamine.Catalytic reduction using a Pd/C catalyst in EtOH under hydrogenatmosphere gave the corresponding aniline as a light grey solid. ¹H NMR(400 MHz, CDCl₃) δ 7.92 (s, 1H), 7.76 (d, J=8 Hz, 2H), 7.66 (d, J=4.5Hz, 2H), 7.55 (s, 1H), 6.75 (d, J=4.5 Hz, 2H), 3.8 (br s, 2H); EIMS304.0; mp 191° C. Anal. Calcd. for C₁₆H₁₂F₃N₃: C, 63.36; H, 3.99; N,13.85. Found: C, 63.14; H, 4.07; N, 13.52.

Example 53 Preparation of4-[1-(4-trifluoromethoxyphenyl)-1H-imidazol-4-yl]-phenylamine

Step 1. 4-(4-Nitrophenyl)-1-(4-trifluoromethoxy-phenyl)-1H-imidazole.The conditions described by Porretta et al. Farmaco, EdizioneScientifica 1985, 40, 404 were used to convert 4-trifluoromethoxyaniline(5.3 g, 30 mmol) and α-bromo-4-nitroacetophenone (3.7 g, 15 mmol) into2.1 g (41% overall yield) of the imidazole.

Step 2. 4-[1-(4-Trifluoromethoxyphenyl)-1H-imidazol-4-yl]-phenylamine.Catalytic reduction using a Pd/C catalyst in EtOH under hydrogenatmosphere gave the corresponding aniline as a light grey solid. ¹H NMR(300 MHz, CDCl₃) δ 7.83 (s, 1H), 7.64 (d, J=4.8 Hz, 2H), 7.47 (d, J=4.4Hz, 2H), 7.40 (s, 1H), 7.36 (d, J=4.8 Hz, 2H), 6.75 (d, J=4.4 Hz, 2H),3.5 (br s, 2H); EIMS 320; mp 167° C. Anal. Calcd. for C₁₆H₁₂F₃N₃O: C,60.19; H, 3.79; N, 13.16. Found: C, 59.91; H, 3.67; N, 13.03.

Example 54 Preparation of4-(4-aminophenyl)-2-(4-trifluoromethoxy-phenyl)-2,4-dihydro-[1,2,4]triazol-3-one

Step 1.4-(4-Nitrophenyl)-2-(4-trifluoromethoxyphenyl)-2,4-dihydro-[1,2,4]triazol-3-one.The title compound was prepared according to the procedure in Henbach,DE 2724891 A1, 1978, with modifications to three steps: In the additionof the aniline, 4-nitroaniline was used instead of 3,5-dichloroanilineand dry THF was used as solvent instead of toluene. In the formation ofthe triazolinone ring, triphosgene (0.65 equiv) was used instead ofphosgene. ¹H NMR (300 MHz, CDCl₃) δ 8.40 (d, J=8.8 Hz, 2H), 8.05 (d,J=8.8 Hz, 2H), 7.99 (s, 1H), 7.89 (d, J=9.3 Hz, 2H), 7.32 (d, J=9.3 Hz,2H); ESIMS 367 (M+H); mp 136-140° C.

Step 2.4-(4-Aminophenyl)-2-(4-trifluoromethoxyphenyl)-2,4-dihydro-[1,2,4]triazol-3-one.The nitrophenyl triazolinone (0.037 g, 0.10 mmol) was dissolved inabsolute EtOH (1 mL) under N₂. To this was added tin(II) chloridedihydrate (0.114 g, 0.51 mmol), and the mixture was stirred at refluxfor 2 h. The mixture was cooled to 25° C., was poured onto ice-H₂O (25mL), and the aqueous mixture was brought to pH 9-10 with 1 N NaOH. Themixture was extracted with Et₂O (3×25 mL), and the combined organicextracts were dried (MgSO₄), filtered and concentrated to give a darkbrown solid (0.0297 g, 87%) that was used without further purification.¹H NMR (300 MHz, CDCl₃) δ 8.07 (d, J=9.7 Hz, 2H), 7.73 (s, 1H),7.32-7.23 (m, 4H), 6.77 (d, J=8.5 Hz, 2H), 3.85 (br, 2H); ESIMS 336(M⁺); mp 115-120° C.

Example 55 Preparation of4-[5-(4-trifluoromethylphenyl)-4,5-dihydro-isoxazol-3-yl]-phenylamine

Step 1.{4-[5-(4-Trifluoromethylphenyl)-4,5-dihydro-isoxazol-3-yl]-phenyl}-carbamicacid tert-butyl ester. To a stirred solution of N-chlorosuccinimide (57mg, 0.424 mmol) and pyridine (3 μL) in 1.7 mL of chloroform was added4-N-t-BOC-aminobenzaldehyde oxime (100 mg, 0.424 mmol). The reaction wasstirred at room temperature for 10 min. 4-Trifluoromethylstyrene (78 μL,0.53 mmol) was then added and the temperature was increased to 45° C. Tothis solution was added triethylamine (62 μL, 0.445 mmol) dissolved in0.5 mL of CHCl₃ dropwise. The reaction was stirred at 45° C. for 5 h.The cooled solution was diluted with chloroform (10 mL) and washed withwater (2×5 mL). The organic phase was then dried over MgSO₄, filteredand concentrated to give the isoxazoline (100 mg, 58%). ¹H NMR (400 MHz,CDCl₃) δ 7.40-7.83 (m, 8H), 6.60 (bs, 1H), 5.76 (dd, J=11.0, 7.7 Hz,1H), 3.81 (dd, J=16.5, 11.0 Hz, 1H), 3.29 (dd, J=16.5, 7.7 Hz, 1H); EIMS406 (M⁺).

Step 2.4-[5-(4-Trifluoromethylphenyl)-4,5-dihydro-isoxazol-3-yl]-phenylamine.To a stirred solution of the N-BOC isoxazoline (prepared in step 1) inCH₂Cl₂ (2.5 mL) was added trifluoroacetic acid (6.16 mmol, 0.46 mL) andthe reaction was stirred at room temperature for 3 h. The solution wasconcentrated and the residue was taken up in 5 mL of saturated KHCO₃solution and stirred for 30 min. The mixture was then extracted withCH₂Cl₂ (3×10 mL). The organic phase was then dried over MgSO₄, filteredand concentrated to afford the expected aniline (68 mg, 90%). ¹H NMR(400 MHz, CDCl₃) δ 7.45-7.63 (m, 6H), 6.67 (d, J=8.6 Hz, 2H), 5.72 (dd,J=10.9, 7.6 Hz, 1H), 3.92 (bs, 2H), 3.78 (dd, J=16.7, 10.9 Hz, 1H), 3.25(dd, J=16.7, 7.6 Hz, 1H); EIMS 306 (M⁺).

Example 56 Preparation of4-[3-(4-Trifluoromethoxyphenyl)-4,5-dihydro-isoxazol-5-yl]-phenylamine

To a stirred solution of N-chlorosuccinimde (0.634 mmol, 85 μL) andpyridine (4 μL) in 2.5 mL of chloroform was addedp-trifluoromethoxybenzaldehyde oxime (130 mg, 0.634 mmol). The reactionwas heated at 50° C. for 3 h. 4-Aminostyrene (0.793 mmol, 93 μL) wasthen added followed by a solution of triethylamine (0.666 mmol, 93 μL)dissolved in 0.5 mL of CHCl₃ dropwise. The reaction was stirred at 50°C. for 3 h. The cooled solution was diluted with chloroform (15 mL) andwashed with water (2×10 mL). The organic phase was then dried overMgSO₄, filtered and concentrated. The residue was purified via radialchromatography using a 2:1 hexane/EtOAc solution as the eluent(R_(f)=0.18) to afford4-[3-(4-trifluoromethoxyphenyl)-4,5-dihydro-isoxazol-5-yl]-phenylamine(125 mg; 61%). ¹H NMR (400 MHz, CDCl₃) δ 7.73 (d, J=8.2 Hz, 2H), 7.25(d, J=8.2 Hz, 2H), 7.17 (d, J=8.2 Hz, 2H), 6.68 (d, J=8.2 Hz, 2H), 5.65(dd, J=10.9, 8.9 Hz, 1H), 3.55-3.75 (bs, 2H), 3.67 (dd, J=16.8, 10.9 Hz,1H), 3.30 (dd, J=16.8, 8.9 Hz, 1H); EIMS 322 (M⁺).

Example 57 Preparation of1-(4-aminophenyl)-3-(4-trifluoromethoxy-phenyl)-1,3-dihydro-imidazol-2-one.

These compounds were prepared according to the procedure described inBromidge et al. WO 2003057220 A1 with slight modifications.

Step 1. (2,2-Dimethoxyethyl)-(4-trifluoromethoxyphenyl) amine. To astirred solution of 4-trifluoromethoxyaniline (1 mL, 7.46 mmol) andglyoxaldehyde diemethyl acetal (60% v/v in water, 8.95 mmol, 1.6 mL) in37 mL of EtOH was added 300 mg of 10% palladium on carbon. The mixturewas evacuated and flushed with nitrogen three times. Hydrogen was thenadded in a balloon apparatus and the mixture was stirred under 1 atm ofhydrogen for 31 h. The mixture was then filtered through a pad ofCelite® and the pad was washed with EtOH (25 mL). The ethanol wasremoved under reduced pressure and the residue was diluted with 30 mL ofCH₂Cl₂. The layers were separated and the organic phase was dried overMgSO₄, filtered and concentrated to give(2,2-dimethoxyethyl)-(4-trifluoromethoxyphenyl) amine (1.7 g, 86%). ¹HNMR (400 MHz, CDCl₃) δ 7.04 (d, J=8.9 Hz, 2H), 6.59 (d, J=8.9 Hz, 2H),4.56 (t, J=5.4 Hz, 1H), 3.92 (bs, 1H), 3.51 (d, J=5.4 Hz, 2H), 3.42 (s,6H); EIMS 265 (M⁺).

Step 2.1-(2,2-Dimethoxyethyl)-3-(4-nitrophenyl)-1-(4-trifluoromethoxyphenyl)-urea.To a stirred solution of (2,2-dimethoxyethyl)-(4-trifluoromethoxyphenyl)amine (3.2 mmol, 0.85 g) dissolved in 32 mL of CH₂Cl₂ was addedp-nitrophenyl isocyanate (3.53 mmol, 0.58 g) and the reaction wasstirred at room temperature overnight. The mixture was diluted withCH₂Cl₂ (50 mL) and was washed successively with NaHCO₃ (30 mL) and brine(30 mL). The organic phase was then dried over MgSO₄, filtered andconcentrated. The residue was purified via radial chromatography using a2:1 hexane/EtOAc solution as the eluent (R_(f)=0.32) to afford1-(2,2-dimethoxyethyl)-3-(4-nitrophenyl)-1-(4-trifluoromethoxyphenyl)-urea(0.87 g, 63%). ¹H NMR (400 MHz, CDCl₃) δ 8.15 (d, J=9.2 Hz, 2H),7.30-7.50 (m, 6H), 7.02 (bs, 1H), 4.65 (t, J=5.4 Hz, 1H), 3.82 (d, J=5.4Hz, 2H), 3.41 (s, 6H); EIMS 429 (M⁺).

Step 3.1-(4-Nitrophenyl)-3-(4-trifluoromethoxyphenyl)-1,3-dihydroimidazol-2-one.To a stirred solution of1-(2,2-dimethoxyethyl)-3-(4-nitrophenyl)-1-(4-trifluoromethoxyphenyl)-urea(0.23 g, 0.53 mmol) dissolved in 28 mL of toluene was added 2 drops ofconcentrated HCl. The reaction mixture was stirred at reflux for 3 h.The cooled solution was diluted with EtOAc (75 mL) and washed withsaturated NaHCO₃ (25 mL) and brine (25 mL). The organic phase was thendried over MgSO₄, filtered and concentrated. The residue was purifiedvia radial chromatography using a 2:1 hexane/EtOAc solution as theeluent (R_(f)=0.28) to afford1-(4-nitrophenyl)-3-(4-trifluoromethoxyphenyl)-1,3-dihydroimidazol-2-one(134 mg, 71%). ¹H NMR (400 MHz, CDCl₃) δ 8.35 (d, J=9.2 Hz, 2H), 7.93(d, J=9.2 Hz, 2H), 7.67 (d, J=9.2 Hz, 2H), 7.34 (d, J=9.2 Hz, 2H), 6.87(d, J=3.3 Hz, 1H), 6.81 (d, J=3.3 Hz, 1H); EIMS 365 (M⁺).

Step 4.1-(4-Aminophenyl)-3-(4-trifluoromethoxyphenyl)-1,3-dihydro-imidazol-2-one.To a stirred solution of1-(4-nitrophenyl)-3-(4-trifluoro-methoxyphenyl)-1,3-dihydroimidazol-2-one(120 mg, 0.33 mmol) in 3.5 mL of EtOAc was added tin dichloride (371 mg,1.64 mmol) and the reaction mixture was stirred at reflux for 3 h. Thecooled solution was poured onto ice (15 mL) and the pH was adjusted topH 7-8 by the addition of 10% NaHCO₃. The mixture was extracted withEtOAc (3×10 mL) and washed with brine (10 mL). The organic phase wasthen dried over MgSO₄, filtered and concentrated to obtain1-(4-amino-phenyl)-3-(4-trifluoromethoxyphenyl)-1,3-dihydro-imidazol-2-one.(102 mg, 92%). ¹H NMR (400 MHz, CDCl₃) δ 7.72 (d, J=8.8 Hz, 2H), 7.37(d, J=8.8 Hz, 2H), 7.32 (d, J=8.8 Hz, 2H), 6.76 (d, J=8.8 Hz, 2H), 6.69(d, J=3.3 Hz, 1H), 6.65 (d, J=3.3 Hz, 1H); EIMS 335 (M⁺).

Example 58 Preparation of1-(4-aminophenyl)-3-(4-trifluoromethoxyphenyl)-imidazolidin-2-one

To a solution of1-(4-nitrophenyl)-3-(4-trifluoromethoxyphenyl)-1,3-dihydroimidazol-2-one(144 mg, 0.395 mmol) in 40 mL of EtOH was added 100 mg of 10% palladiumon carbon. The mixture was evacuated and flushed with nitrogen threetimes. The Parr vessel was pressurized to 45 psi of hydrogen and shakenfor 5 h. The depressurized solution was filtered through a pad ofCelite® and the pad was washed with EtOH (25 mL). The ethanol wasremoved under reduced pressure to afford the title product (114 mg,95%). ¹H NMR (400 MHz, CDCl₃) δ 7.61 (d, J=9.2 Hz, 2H), 7.33 (d, J=9.2Hz, 2H), 7.21 (d, J=8.6 Hz, 2H), 6.71 (d, J=9.2 Hz, 2H), 3.92 (s, 4H),3.61 (bs, 2H); EIMS 307 (M⁺).

Example 59 Preparation of4-[6-(4-trifluoromethoxyphenyl)-pyridazin-3-yl]-phenylamine

Step 1. 3-Chloro-6-(4-trifluoromethoxyphenyl)-pyridazine. To a solutioncontaining 3,6-dichloropyridazine (0.3 g, 2.01 mmol),4-trifluoromethoxyphenyl-boronic acid (0.50 g, 2.42 mmol) and 2 M K₂CO₃(2 mL, 4.03 mmol) dissolved in 11 mL of dry 1,4-dioxane was addeddichlorobis(triphenylphosphine)palladium(II) (14 mg, 0.02 mmol). Themixture was irradiated using a CEM Discover microwave at 190° C. for 30min. The mixture was diluted with 100 mL of ether and washed with brine(30 mL). The organic phase was then dried over MgSO₄, filtered andconcentrated. The residue was purified via radial chromatography using a3:1 hexane/EtOAc solution as the eluent. Two fractions were isolated.The first fraction (R_(f)=0.63) was shown to be the bis-Suzuki product(95 mg, 12%). The second fraction isolated (R_(f)=0.34) was identifiedas 3-chloro-6-(4-trifluoromethoxyphenyl)-pyridazine (174 mg, 32%).

¹H NMR (400 MHz, CDCl₃) δ 8.10 (d, J=9.2 Hz, 2H), 7.83 (d, J=8.9 Hz,2H), 7.60 (d, J=8.9 Hz, 2H), 7.37 (d, J=9.2 Hz, 2H); EIMS 274 (M⁺).

Step 2. 4-[6-(4-Trifluoromethoxyphenyl)-pyridazin-3-yl]-phenylamine.

To a solution containing3-chloro-6-(4-trifluoromethoxyphenyl)-pyridazine (157 mg, 0.57 mmol),4-aminophenylboronic acid (118 mg, 0.86 mmol) and 2 M K₂CO₃ (0.57 mL,1.14 mmol) dissolved in 3.5 mL of dry 1,4-dioxane was addeddichlorobis(triphenylphosphine)palladium(II) (4 mg, 0.006 mmol). Themixture was irradiated using a CEM Discover microwave at 190° C. for 30min. The mixture was diluted with 100 mL of ether and washed with brine(30 mL). The organic phase was then dried over MgSO₄, filtered andconcentrated. The residue was purified via radial chromatography using a97:3 CHCl₃/CH₃OH solution as the eluent (R_(f)=0.26) to afford the titlecompound (105 mg, 56%). ¹H NMR (400 MHz, CDCl₃) δ 8.18 (d, J=8.6 Hz,2H), 8.01 (d, J=8.6 Hz, 2H), 7.30-7.45 (m, 4H), 6.82 (d, J=8.6 Hz, 2H),3.96 (bs, 2H); EIMS 331 (M⁺).

Example 60 Preparation of4-[3-(4-Trifluoromethoxyphenyl)-4-5-dihydro-[1,2,4]oxadiazol-5-yl]-benzaldehyde

The compound was prepared according to the general procedure ofSrivastava et al. J. Heterocycl. Chem. 1987, 24, 101 with slightmodifications. To a stirred solution of4-(trifluoromethoxy)benzamidoxime (Acros) (300 mg, 1.36 mmol) dissolvedin 1.4 mL of acetic acid was added 1,4-terephthaldehyde (1.1 g, 8.18mmol) and the reaction was stirred at room temperature for 4 d. Themixture was then dissolved in CHCl₃ (20 mL) followed by addition of 10mL of heptane. This solution was concentrated under reduced pressure.This procedure was repeated twice. The residue was purified via radialchromatography using a 99:1 CHCl₃/CH₃OH solution as the eluent. Twofractions were isolated. The first fraction isolated (R_(f)=0.30) wasshown to be starting material (20 mg). The second fraction isolated(R_(f)=0.17) was shown to be the title compound (23 mg, 5%). ¹H NMR (400MHz, CDCl₃) δ 10.02 (s, 1H), 7.91 (d, J=8.2 Hz, 2H), 7.77 (d, J=9.2 Hz,2H), 7.70 (d, J=8.2 Hz, 2H), 7.27 (d, J=8.2 Hz, 2H), 6.64 (d, J=4.3 Hz,1H), 5.18 (d, J=4.3 Hz, 1H); EIMS 336 (M⁺).

Example 61 Preparation of4-[5-(4-Trifluoromethoxyphenyl)-[1,2,4]oxadiazol-3-yl]-phenylamine

Step 1.{4-[5-(4-Trifluoromethoxyphenyl)-[1,2,4]oxadiazol-3-yl]-phenyl}-carbamicacid tert-butyl ester. To a stirred solution oftert-butyl-4-(N-hydroxycarbamimidoyl)-phenylcarbamate (Ace Synthesis)(500 mg; 1.99 mmol) dissolved in 2.5 mL of acetic acid was added4-trifluoromethoxybenzaldehyde (1.7 mL; 11.94 mmol), and the reactionmixture was stirred at room temperature for 4 d. The mixture was dilutedwith CHCl₃ (20 mL) and filtered through a pad of Celite®. The pad waswashed with CHCl₃ (20 mL). Heptane (20 mL) was then added to thesolution and the solution was concentrated under reduced pressure. Thisprocedure was repeated twice. The residue was purified via radialchromatography using a 3:1 hexane/EtOAc solution as the eluent. Twofractions were isolated. The first fraction isolated (R_(f)=0.42) wasshown to be the title compound (127 mg; 15%). ¹H NMR (300 MHz, CDCl₃) δ8.26 (d, J=8.9 Hz, 2H), 8.09 (d, J=8.9 Hz, 2H), 7.52 (d, J=8.6 Hz, 2H),7.39 (d, J=8.3 Hz, 2H), 6.70 (s, 1H), 1.54 (s, 9H); EI/MS 421 [M]⁺. Thesecond fraction isolated (R_(f)=0.11) was shown to be the4,5-dihydro-1,2,4-oxadiazole (96 mg; 11%). ¹H NMR (300 MHz, CDCl₃) δ8.40(d, J=8.9 Hz, 2H), 8.00 (d, J=8.9 Hz, 2H), 7.51 (d, J=8.9 Hz, 2H),7.22-7.31 (m, 3H), 6.87 (s, 1H), 1.54 (s, 9H); EI/MS 423 [M]⁺.

Step 2.4-[5-(4-Trifluoromethoxyphenyl)-[1,2,4]oxadiazol-3-yl]-phenylamine. To astirred solution of{4-[5-(4-trifluoromethoxyphenyl)-[1,2,4]oxadiazol-3-yl]-phenyl}-carbamicacid tert-butyl ester (198 mg; 0.47 mmol) in CH₂Cl₂ (4.7 mL) was addedtrifluoroacetic acid (11.76 mmol; 0.87 mL) and the reaction was stirredat room temperature for 3 h. The solution was concentrated and theresidue was taken up in 10 mL of saturated KHCO₃ solution and stirredfor 30 min. The mixture was then extracted with CH₂Cl₂ (3×10 mL). Theorganic phase was then dried over MgSO₄, filtered and concentrated toafford4-[5-(4-trifluoromethoxyphenyl)-[1,2,4]oxadiazol-3-yl]-phenylamine (127mg; 84%). ¹H NMR (300 MHz, CDCl₃) δ 8.26 (d, J=8.9 Hz, 2H), 7.97 (d,J=8.9 Hz, 2H), 7.39 (d, J=8.6 Hz, 2H), 6.77 (d, J=8.6 Hz, 2H), 3.40-3.80(bs, 2H); EI/MS 321 [M]⁺.

Example 62 Preparation of1-(4-amin-phenyl)-4-(4-trifluoromethoxy-phenyl)-piperazine-2,5-dione

Step 1. 4-Nitrophenylamino acetic acid, methyl ester. To a solution ofethyl bromoacetate (60 g, 0.36 mol) and 4-nitroaniline (5 g, 0.036 mol)in 100 mL of DMF was added NaHCO₃ (60 g, 0.71 mol) andtetra-n-butylammonium iodide (500 mg, cat). The solution was heated to90° C. for 16 h, and then it was cooled and poured onto 300 mL of water.The resulting yellow solid was filtered and air-dried. Recrystallizationfrom MeOH furnished 5 g of the methyl ester as a light yellow solid. ¹HNMR (400 MHz, CDCl₃) δ 8.36 (d, J=8 Hz, 2H), 7.65 (d, J=8 Hz, 2H), 4.42(2, 2H), 3.93 (s, 2H), 3.79 (s, 2H); mp 179-182° C.

Step 2. [(2-Chloroacetyl)-(4-trifluoromethoxyphenyl)-amino]-acetic acidmethyl ester. To a suspension of 4-nitrophenylamino acetic acid, methylester (3.0 g, 14.2 mmol) in 30 mL of toluene was added chloroacetylchloride (3 mL, excess). The solution was heated to 80° C. for 1 h,whereupon the solid dissolved. The solution was then cooled andconcentrated, and then the residual solid was recrystallized from MeOHto give 3.5 g of the ester as a light yellow solid. ¹H NMR (400 MHz,CDCl₃) δ 8.36 (d, J=8 Hz, 2H), 7.65 (d, J=8 Hz, 2H), 4.42 (2, 2H), 3.93(s, 2H), 3.79 (s, 3H); MS 286 (M⁺); mp 106-109° C.

Step 3.1-(4-Aminophenyl)-4-(4-trifluoromethoxyphenyl)-piperazine-2,5-dione. Theproduct of step 2 (0.6 g, 2.3 mmol) was combined with4-trifluoromethoxyaniline (0.81 g, 4.6 mmol) and the materials wereheated to 140° C. for 90 min. The residual solid was stirred with 50 mLof DCM and filtered to remove the hydrochloride salt of the aniline, andthen the residue was concentrated and purified. Chromatography (elutionwith EtOAc-hexanes) furnished 0.44 g of the nitrophenyl piperazinedioneas a white solid, mp 223-224° C. Reduction of the nitro group using aPd/C catalyst under conditions described above gave the title amine as awhite solid. ¹H NMR (400 MHz, CDCl₃) δ 7.4 (d, J=8.5 Hz, 2H), 7.33 (d,J=8.6 Hz, 2H), 7.12 (d, J=8.7 Hz, 2H), 6.75 (d, J=8.7 Hz, 2H), 4.5 (s,2H), 4 45 (s, 2H); MS 366.2 (M+H⁺); mp 250° C. (dec.).

Example 63 Preparation of5-(4-aminophenyl)-3-(4-trifluoromethylphenyl)-3H-[1,3,4]oxadiazol-2-one

5-(4-Nitrophenyl)-3-(4-trifluoromethylphenyl) 3H-[1,3,4]oxadiazole-2-onewas prepared by treating the corresponding 4-nitrobenzoic acid,N′-(4-trifluoromethylphenyl)-hydrazide with phosgene, using conditionsdescribed by Reimlinger, et al, in Chemische Berichte 1970, 103, 1934.The nitro group was then reduced to the amine by treatment with hydrogenand Pd/C in EtOH. ¹H NMR (400 MHz, CDCl₃) δ 8.1 (d, J=8.4 Hz, 2H), 7.75(m, 4H), 6.75 (d, J=8.4 Hz, 2H), 4.1 (br s, 2H); MS 322.6 (M+H⁺); mp160-163° C.

Example 64 Preparation of4-[1-(4-Trifluoromethoxyphenyl)-1H-imidazol-4-yl]-benzaldehydeO-((2S,3R,4R,5S,6S)-3,4,5-trimethoxy-6-methyl-tetrahydropyran-2-yl)-oxime(Compound 26)

A solution of4-[1-(4-trifluoromethoxyphenyl)-1H-imidazol-4-yl]-benzaldehyde (50 mg,0.15 mmol) andO-(2S,3R,4R,5S,6S)-(3,4,5-trimethoxy-6-methyl-tetrahydropyran-2-yl)-hydroxylamine(45 mg, 0.20 mmol) were combined in 5 mL of dry EtOH, and the solutionheated at reflux under a N₂ atmosphere for 12 h. The resulting solutionwas concentrated in vacuo and purified by chromatography (Biotage, 1:1:1Hexanes/EtOAc/DCM) to furnish 35 mg (44%) of Compound 26 as a whitesolid. ¹H NMR (300 MHz, CDCl₃) δ 8.15 (s, 1H), 7.90 (s, 1H), 7.85 (d,J=6 Hz, 2H), 7.68 (d, J=6 Hz, 2H), 7.60 (s, 1H), 7.68 (s, 1H), 7.50 (d,J=6 Hz, 2H), 7.38 (d, J=6 Hz, 2H), 3.77 (dd, J=3.2, 2.0 Hz, 1H), 3.68(dd, J=9.6, 6.2 Hz, 1H), 3.59 (s, 3H), 3.56 (s, 3H), 3.55 (s, 3H), 3.51(m, 1H), 3.21 (t, J=9.3 Hz, 1H), 1.33 (d, J=6.1 Hz, 3H); MS 536.1 (M+H);mp 178° C. Anal. Calcd. for C₁₆H₁₀F₃N₃O₂: C, 59.01; H, 5.50; N, 7.65.Found: C, 58.86; H, 5.58; N, 7.63.

The compounds of this invention in Table 4 were prepared by the routesdescribed earlier and illustrated in Example 64.

Example 65 Preparation of2,2,2-trifluoro-1-{4-[1-(4-trifluoromethyl-phenyl)-1H-[1,2,4]triazol-3-yl]-phenyl}-ethanone,O-((2S,3R,4R,5S,6S)4-ethoxy-3,5-dimethoxy-6-methyl-tetrahydropyran-2-yl)-oxime (Compound169)

The oxime was prepared from the correspondingtrifluoromethylacetophenone using the conditions described in theprevious Examples. ¹H NMR (300 MHz, CDCl₃) δ 8.68 (s, 1H), 8.26 (d,J=8.30 Hz, 2H), 7.88 (d, J=8.26 Hz, 2H), 7.81 (d, J=8.26 Hz, 2H), 7.68(d, J=8.30 Hz, 2H), 5.63 (d, J=1.85 Hz, 1H), 3.79-3.61 (m, 4H), 3.57 (s,3H), 3.56 (s, 3H), 3.44 (dd, J=9.31, 3.36 Hz, 1H), 3.18 (t, J=9.48 Hz,1H), 1.36-1.23 (m, 6H); MS 602 ([M+H]⁺).

The compounds of this invention in Table 5 were prepared by the routesdescribed earlier and illustrated in Examples 64 and 65.

Example 66 Preparation of5-[1-(4-trifluoromethoxyphenyl)-1H-[1,2,4]triazol-3-yl]-indan-1-oneO-((2S,3R,4R,5S,6S)-4-ethoxy-3,5-dimethoxy-6-methyl-tetrahydropyran-2-yl)-oxime(Compound 170)

The oxime was prepared from the corresponding 2-indanone using theconditions described in Example 64. ¹H NMR (300 MHz, CDCl₃) δ 8.62 (s,1H), 8.22-8.16 (m, 2H), 7.84-7.78 (m, 3H), 7.42-7.38 (m, 2H), 5.63 (d,J=1.85 Hz, 1H), 3.79-3.61 (m, 4H), 3.57 (s, 3H), 3.56 (s, 3H), 3.44 (dd,J=9.31, 3.36 Hz, 1H), 3.22-3.18 (m, 3H), 3.02-2.96 (m, 2H), 1.36-1.23(m, 6H); MS 576 ([M+H]⁺).

Example 67 Preparation of4-{1-[5-(1,1,2,3,3,3-hexafluoropropoxy)-pyridinyl]-1H-[1,2,4]triazol-3-yl}-benzaldehydeO-((2S,3R,4R,5S,6S)-3,4,5-trimethoxy-6-methyl-tetrahydropyran-2-yl)-oxime(Compound 94)

Fluoroalkylation conditions were based on a paper by Timperley et al. J.Fluorine Chem. 2006, 127, 249. A solution of4-[1-(5-hydroxy-pyridin-2-yl)-1H-[1,2,4]triazol-3-yl]-benzaldehydeO-((2S,3R,4R,5S,6S)-3,4,5-trimethoxy-6-methyl-tetrahydropyran-2-yl)-oximein 10 mL anhydrous DMF/THF (1:1) under a N₂ atmosphere was cooled at 0°C. while an excess of hexafluoropropylene gas was added over 15 min.Following addition, triethylamine (15 uL, 0.109 mmol) was added and thereaction mixture warmed to ambient temperature before concentration todryness. Chromatography (EtOAc/hexanes, 1:1) afforded Compound 94 (16mg, 24%). ¹H NMR (CDCl₃) δ 9.17 (s, 1H), 8.39 (d, J=7.68 Hz, 1H), 8.21(d, J=8.22 Hz, 2H), 8.19 (s, 1H), 8.08 (d, J=7.68 Hz, 1H), 7.74 (d,J=8.22 Hz, 2H), 6.97 (s, 1H), 5.63 (d, J=1.85 Hz, 1H), 5.17 (m, 1H),3.78 (dd, J=3.28, 1.99 Hz, 1H), 3.63 (m, 1H), 3.59 (s, 3H), 3.57 (s,3H), 3.56 (s, 3H), 3.43 (dd, J=9.31, 3.36 Hz, 1H), 3.18 (t, J=9.48 Hz,1H), 1.29 (d, J=6.26 Hz, 3H); EIMS 619 m/z (M⁺).

Example 68 Preparation of4-[1-(4-trifluoromethanesulfinylphenyl)-1H-[1,2,4]triazol-3-yl]-benzaldehydeO-((2S,3R,4R,5S,6S)-3,4,5-trimethoxy-6-methyl-tetrahydropyran-2-yl)-oxime(Compound 103) and4-[1-(4-trifluoromethanesulfonylphenyl)-1H-[1,2,4]triazol-3-yl]-benzaldehydeO-((2S,3R,4R,5S,6S)-3,4,5-trimethoxy-6-methyl-tetrahydropyran-2-yl)-oxime(Compound 104)

A solution of4-[1-(4-trifluoromethylsulfanylphenyl)-1H-[1,2,4]triazol-3-yl]-benzaldehydeO-((2S,3R,4R,5S,6S)-3,4,5-trimethoxy-6-methyl-tetrahydropyran-2-yl)-oxime(100 mg, 0.18 mmol, 1.0 eq) and 3-chloroperoxybenzoic acid (124 mg, 0.72mmol, 4.0 eq) in DCM (10 mL) was stirred under ambient conditions for 48h. The solution was then washed with saturated NaHSO₃ (aq), extractedinto DCM (100 mL), concentrated to dryness, and purified viachromatography (2:2:1, hexanes/EtOAc/acetone) to afford 55 mg of thesulfoxide (54%) and the sulfone (5.6 mg, 5%).

For the sulfoxide (Compound 103): ¹H NMR (CDCl₃) δ 8.78 (s, 1H), 8.26(d, J=8.24 Hz, 2H), 8.21 (s, 1H), 8.09 (d, J=8.38 Hz, 2H), 7.99 (d,J=8.38 Hz, 2H), 7.78 (d, J=8.24 Hz, 2H), 5.63 (d, J=1.85 Hz, 1H), 3.68(dd, J=3.28, 1.99 Hz, 1H), 3.63 (m, 1H), 3.59 (s, 3H), 3.57 (s, 3H),3.56 (s, 3H), 3.44 (dd, J=9.31, 3.36 Hz, 1H), 3.20 (t, J=9.48 Hz, 1H),1.25 (d, J=6.26 Hz, 3H); EIMS 568 m/z (M⁺).

For the sulfone (Compound 104): ¹H NMR (CDCl₃) δ 8.79 (s, 1H), 8.24-8.18(m, 5H), 8.15 (d, J=8.28 Hz, 2H), 7.79 (d, J=8.32 Hz, 2H), 5.63 (d,J=1.85 Hz, 1H), 3.68 (dd, J=3.28, 1.99 Hz, 1H), 3.63 (m, 1H), 3.59 (s,3H), 3.57 (s, 3H), 3.56 (s, 3H), 3.44 (dd, J=9.31, 3.36 Hz, 1H), 3.20(t, J=9.48 Hz, 1H), 1.25 (d, J=6.26 Hz, 3H); EIMS 584 m/z (M⁺).

Example 69 Preparation of4-[1-(4-pentafluoroethyloxy-phenyl)-1H-[1,2,4]triazol-3-yl]-benzaldehyde,O-((2S,3R,4R,5S,6S)-3,4-dimethoxy-6-methyl-5-propoxy-tetrahydropyran-2-yl)-oxime(Compound 113)

Compound III (60 mg, 0.1 mmol) was dissolved in 1 mL of bromopropane andtreated with 50 mg of powdered KOH and 5 mg of powdered Bu₄NI (excess).The solution was stirred at ambient temperature for 16 h, and then wasdiluted with 10 mL of dry Et₂O, filtered and concentrated. The residuewas eluted through a short silica column to give 25 mg of Compound 113.¹H NMR (CDCl₃) δ 8.61 (s, 1H), 8.23 (d, J=8.1 Hz, 2H), 8.01 (s, 1H),7.85 (d, J=9 Hz, 2H), 7.76 (d, J=8.1 Hz, 2H), 7.42 (d, J=9 Hz, 2H), 7.38(d, J=8.2 Hz, 2H), 5.70 (d, J=1.8 Hz, 1H), 3.8-3.6 (m, 3H), 3.60-3.55(m, 8H), 3.30 (t, J=9.6 Hz, 1H), 1.65 (m, 2H), 1.33 (d, J=7 Hz, 3H),0.98 (t, J=7.5 Hz, 3H); EIMS 615.0 m/z (M⁺); mp 121-128° C.

Example 70 Preparation of4-[2-(4-trifluoromethoxyphenyl)-pyridin-2-yl]-benzaldehyde,O-((2S,3R,4R,5S,6S)-3,4,5-trimethoxy-6-methyl-tetrahydropyran-2-yl)-oxime(Compound 132)

Step 1. 2-Chloro-4-iodopyridine (1.6 mmol), 4-cyanophenyl boronic acid(2.5 mmol), 2 M potassium carbonate (3.3 mmol),tetrakis(triphenyphosphine)palladium(0) (0.01 mmol) and dioxane (8 mL)were combined in a vial and heated by microwave for 10 min at 150° C.The crystallized product was filtered and subsequently dried in vacuo toyield 250 mg of 4-(2-chloropyridin-4-yl)-benzonitrile as yellow needles.¹H NMR (400 MHz, CDCl₃) δ 8.52 (d, J=5.1 Hz, 1H), 7.81 (d, J=8.4 Hz,2H), 7.72 (d, J=8.2 Hz, 2H), 7.55 (m, 1H), 7.43 (dd, J=5.2, 1.4 Hz, 1H);EIMS 214 m/z (M⁺).

Step 2. 4-(2-Chloropyridin-4-yl)-benzonitrile (4.65 mmol) was reducedwith DIBAL under conditions described earlier to give the aldehyde as atan solid. ¹H NMR (400 MHz, CDCl₃) δ 10.11 (s, 1H), 8.50 (d, J=4.8 Hz,1H), 8.02 (d, J=8.3 Hz, 2H), 7.78 (d, J=8.2 Hz, 2H), 7.59 (d, J=1.4 Hz,1H), 7.47 (dd, J=5.2, 1.5 Hz, 1H); EIMS 217 m/z (M⁺).

Step 3. 4-(2-Chloropyridin-4-yl)-benzaldehyde (1.5 mmol) andO-((2S,3R,4R,5S,6S)-3,4,5-trimethoxy-6-methyl-tetrahydropyran-2-yl)-hydroxylamine(1.5 mmol) were combined in EtOH under conditions described above in thepreparation of compound 26 to yield the oxime. ¹H NMR (400 MHz, CDCl₃) δ8.45 (d, J=5.9 Hz, 1H), 8.21 (s, 1H), 7.76 (d, J=8.3 Hz, 2H), 7.65 (d,J=8.3 Hz, 2H), 7.55 (m, 1H), 7.44 (dd, J=5.4, 1.6 Hz, 1H), 5.68 (d,J=1.8 Hz, 1H), 3.78 (dd, J=3.1, 2.0 Hz, 1H), 3.68 (dd, J=9.6, 6.3 Hz,1H), 3.59 (s, 3H), 3.56 (s, 3H), 3.55 (s, 3H), 3.52 (m, 1H), 3.21 (t,J=9.5 Hz, 1H), 1.32 (d, J=6.2 Hz, 3H); EIMS 420 m/z (M⁺).

Step 4. 4-[2-(4-Trifluoromethoxyphenyl)-pyridin-4-yl]-benzaldehydeO-((2S,3R,4R,5S,6S)-3,4,5-trimethoxy-6-methyl-tetrahydropyran-2-yl)-oxime.4-(2-Chloropyridin-4-yl)-benzaldehydeO-((2S,3R,4R,5S,6S)-3,4,5-trimethoxy-6-methyl-tetrahydropyran-2-yl)-oxime(0.24 mmol), 4-trifluoromethoxyphenyl boronic acid (0.36 mmol),(Ph₃P)₄Pd(0) (0.002 mmol), 2 M K₂CO₃ (0.475 mmol) and dioxane (1 mL)were combined in a vial and heated by microwave for 10 min at 150° C.The reaction mixture was taken up in ether and washed with brine. Theether layer was dried over magnesium sulfate, was filtered and thesolvent was removed in vacuo. The crude mixture was purified by silicagel chromatography to yield 48 mg of Compound 132 as a tan oil. ¹H NMR(400 MHz, CDCl₃) δ 8.76 (d, J=5.0 Hz, 1H), 8.21 (s, 1H), 8.09 (d, J=8.8Hz, 2H), 7.91 (s, 1H), 7.78 (d, J=8.6 Hz, 2H), 7.72 (d, J=8.7 Hz, 2H),7.48 (dd, J=5.3, 1.7 Hz, 1H), 7.34 (d, J=8.6 Hz, 2H), 5.69 (d, J=1.7 Hz,1H), 3.78 (m, 1H), 3.69 (m, 1H), 3.59 (s, 3H), 3.57 (s, 3H), 3.55 (s,3H), 3.52 (d, J=3.3 Hz, 1H), 3.22 (t, J=9.4 Hz, 1H), 1.33 (d, J=6.2 Hz,3H); EIMS 546 m/z (M⁺).

Example 71 Preparation of{4-[2-(4-trifluoromethylphenyl)-pyrimidin-4-yl]-phenyl}-carbamic acid(2S,3R,4R,5S,6S)-3,4,5-trimethoxy-6-methyl-tetrahydropyran-2-yl ester(Compound 232)

Step 1. Carbonic acid 4-nitrophenyl ester(2S,3R,4R,5S,6S)-3,4,5-trimethoxy-6-methyl-tetrahydropyran-2-yl ester.To a solution cooled in an ice bath of 509 mg (2.52 mmol) of4-nitrophenyl chloroformate in 2 mL of dioxane was added dropwise viasyringe a solution of 0.50 g (2.42 mmol) of3,4,5-trimethoxy-6-methyl-tetrahydropyran-2-ol in 3 mL of pyridine. Thecontents were allowed to gradually warm to room temperature and stirovernight. The pyridine was removed in vacuo at room temperature and theresidue was triturated with ethyl ether. The mixture was filtered andthe filtrate was dried (MgSO₄). Concentration gave 840 mg of an oilwhich was purified by chromatography on silica gel using 3:2hexanes/EtOAc as eluent to afford 337 mg (37%) of the α-anomericcarbamate as the higher R_(f) component; ¹H NMR (400 MHz, CDCl₃) δ 8.30(d, J=9.3 Hz, 2H), 7.43 (d, J=9.2 Hz, 2H), 6.12 (d, J=2.3 Hz, 1H),3.73-3.71 (m, 2H), 3.58 (s, 3H), 3.56 (s, 3H), 3.56 (s, 3H), 3.52 (m,1H), 3.23 (t, J=9.2 Hz, 1H), 1.36 (d, J=6.2 Hz, 3H); and 157 mg (17%) ofthe β-anomeric carbamate as the lower R_(f) component; ¹HNMR NMR (300MHz, CDCl₃) δ 8.32 (d, J=9.3 Hz, 2H), 7.42 (d, J=9.3 Hz, 2H), 5.57 (d,J=2.1 Hz, 1H), 3.87 (m, 1H), 3.71 (s, 3H), 3.59 (s, 3H), 3.56 (s, 3H),3.43 (m, 1H), 3.31-3.18 (m, 2H), 1.43 (d, J=6.2 Hz, 3H); mp 113-116° C.

Step 2. To a mixture cooled in an ice bath of 126 mg (0.40 mmol) of4-[2-(4-trifluoromethylphenyl)-pyrimidin-4-yl]-phenylamine in 1 mL ofdry toluene was added dropwise via syringe 1.6 mL (0.80 mmol) of a 0.5 Msolution of potassium hexamethyldisilazide in toluene over a 10-15minute period. To this mixture was then added dropwise a solution of 148mg (0.400 mmol) of carbonic acid 4-nitrophenyl ester3,4,5-trimethoxy-6-methyl-tetrahydropyran-2-yl ester in 2 mL of toluene.The contents were allowed to gradually warm to room temperature and stirovernight and were added to cold saturated sodium bicarbonate. Themixture was extracted two times with chloroform and the combinedextracts were dried (MgSO₄). Concentration gave 130 mg which waspurified by chromatography on silica gel using 9:1 DCM/EtOAc to afford64 mg (29%) of Compound 232. ¹HNMR (300 MHz, CDCl₃) δ 8.87 (d, J=5.2 Hz,1H), 8.71 (d, J=8.2 Hz, 2H), 8.26 (d, J=8.8 Hz, 2H), 7.79 (d, J=8.2 Hz,2H), 7.65 (d, J=5.2 Hz, 1H), 7.63 (d, 2H), 6.86 (br s, 1H), 6.26 (d,J=1.9 Hz, 1H), 3.74-3.70 (m, 2H), 3.61 (s, 3H), 3.60 (s, 3H), 3.57 (s,3H), 3.53 (m, 1H), 3.24 (t, J=9.5 Hz, 1H), 1.36 (d, J=6.0 Hz, 3H); MS(API-ES+) 549 ([M+H]⁺, 10), 358 (100); mp 176-179° C.

Example 72 Preparation of{4-[2-(4-methoxyphenyl)-pyrimidin-4-yl]-phenyl}-carbamic acid(2S,3R,4R,5S,6S)-3,4,5-trimethoxy-6-methyl-tetrahydropyran-2-yl ester(Compound 234)

To a mixture cooled in an ice bath of 112 mg (0.404 mmol) of4-[2-(4-methoxyphenyl)-pyrimidin-4-yl]-phenylamine in 1.5 mL of dry THFwas added dropwise via syringe 0.81 mL (0.40 mmol) of a 0.5 M solutionof potassium hexamethyldisilazide in toluene over a 10-15 minute period.This solution was then added dropwise via syringe to a solution cooledin an ice bath of 126 mg (0.386 mmol) of carbonic acid 4-nitrophenylester 3,4,5-trimethoxy-6-methyl-tetrahydropyran-2-yl ester in 2 mL ofTHF. The contents were allowed to gradually warm to room temperature andstir overnight and were added to cold saturated sodium bicarbonate. Themixture was extracted two times with ethyl ether and the combinedextracts were dried (MgSO₄). Concentration gave a red oil which waspurified by chromatography on silica gel using 1:1 hexanes/EtOAc toafford 16 mg (8%) of Compound 234. ¹H NMR (300 MHz, CDCl₃) δ 8.79 (d,J=5.2 Hz, 1H), 8.55 (d, J=8.8 Hz, 2H), 8.25 (d, J=8.8 Hz, 2H), 7.62 (d,J=8.5 Hz, 2H), 7.53 (d, J=5.5 Hz, 1H), 7.05 (d, J=9.0 Hz, 2H), 6.84 (brs, 1H), 6.26 (d, J=1.7 Hz, 1H), 3.92 (s, 3H), 3.71-3.69 (m, 2H), 3.61(s, 3H), 3.60 (s, 3H), 3.57 (s, 3H), 3.55-3.47 (m, 1H), 3.24 (t, J=9.4Hz, 1H), 1.36 (d, J=6.1 Hz, 3H); MS (API-ES+) 510 ([M+H]⁺, 100).

Example 73 Preparation of{2-chloro-4-[3-(4-trifluoromethylphenyl)-[1,2,4]triazol-1-yl]-phenyl}-carbamicacid (2S,3R,4R,5S,6S)-3,4,5-trimethoxy-6-methyl-tetrahydropyran-2-ylester (α-anomer, Compound 189), and{2-chloro-4-[3-(4-trifluoromethylphenyl)-[1,2,4]triazol-1-yl]-phenyl}-carbamicacid (2R,3R,4R,5S,6S)-3,4,5-trimethoxy-6-methyl-tetrahydropyran-2-ylester (β-anomer, Compound 190))

A solution of the aniline (0.45 g, 1.3 mmol) in dry THF (5 mL) wastreated with 2 mL of a 20% solution of phosgene in toluene (4 mmol). Thesolution was capped and stored for 18 h, then concentrated andre-dissolved in 5 mL of dry THF. This solution, which was not completelydissolved, was treated with tri-O-methylrhamnopyranoside (0.3 g, 1.45mmol) and triethylamine (0.2 mL, 1.6 mmol), and the solution was heatedto reflux for 1 h. TLC showed the formation of two new, more polarproducts. The solution was concentrated in vacuo, then applied directlyto a Biotage column and eluted with 1:1:1 solution of EtOAc/Hexanes/DCM.The two new products were isolated and concentrated to give 75 mg of theα-anomer (Compound 189) and 110 mg of the β-anomer (Compound 190). Forthe α-anomer: ¹H NMR (300 MHz, CDCl₃) δ 8.60 (s, 1H), 8.41 (d, J=8 Hz,1H), 8.33 (d, J=7.8 Hz, 2H), 7.90 (d, J=1 Hz, 1H), 7.75 (d, J=7.8 Hz,2H), 7.65 (dd, J=1, 8 Hz, 1H), 6.22 (d, J=1.2 Hz, 1H), 3.8-3.65 (m, 2H),3.65-3.5 (m, 10H), 3.22 (t, J=9.2 Hz, 1H), 1.36 (d, J=6.3 Hz, 3H); mp175° C. For the β-anomer: ¹H NMR (300 MHz, CDCl₃) δ 8.60 (s, 1H), 8.38(d, J=8 Hz, 1H), 8.37 (d, J=7.8 Hz, 2H), 7.90 (d, J=1.5 Hz, 1H), 7.75(d, J=7.8 Hz, 2H), 7.65 (dd, J=1.5, 8 Hz, 1H), 7.45 (s, 1H, NH), 5.72(s, 1H), 3.85 (m, 1H), 3.75 (s, 3H), 3.62 (s, 3H), 3.58 (s, 3H), 3.45(m, 1H), 3.35 (m, 1H), 3.22 (t, J=9.2 Hz, 1H), 1.36 (d, J=6.3 Hz, 3H).

Example 74 Preparation of{4-[1-(4-trifluoromethoxyphenyl)-1H-[1,2,4]triazol-3-yl]-phenyl}-carbamicacid (2S,3R,4R,5S,6S)-3,4,5-trimethoxy-6-methyl-tetrahydropyran-2-ylester (Compound 191)

The aniline (0.15 g, 0.47 mmol) was taken up in 5 mL of DCM and treatedwith di-tert-butyl tricarbonate (0.15 g 0.57 mmol). The solution wasallowed to stir magnetically for 1 h, and then it was concentrated invacuo and redissolved in dry THF. To this solution was addedtri-O-methyl rhamnopyranoside (0.13 g, 0.63 mmol) and triethylamine (0.1g, 1 mmol), and the solution was heated to reflux for 1 h, then cooled,concentrated, and purified by chromatography (1:1:1 Hexanes/EtOAc/DCM)to afford 160 mg of Compound 191 as a white solid. ¹H NMR (300 MHz,CDCl₃) δ 8.55 (s, 1H), 8.16 (d, J=8.7 Hz, 2H), 7.79 (d, J=9.1 Hz, 2H),7.53 (d, J=8.7 Hz, 2H), 7.38 (d, J=8.8 Hz, 2H), 6.78 (s, 1H), 6.23 (d,J=1.9 Hz, 1H), 3.70 (m, 2H), 3.59 (s, 3H), 3.57 (s, 3H), 3.54 (s, 3H),3.51 (m, 1H), 3.21 (t, J=9.4 Hz, 1H), 1.34 (d, J=6.2 Hz, 3H); MS 553.0(M+H); mp 186-188° C.

Example 75 Preparation of{4-[1-(4-pentafluoroethyloxyphenyl)-1H-[1,2,4]triazol-3-yl]-phenyl}-carbamicacid(2S,3R,4R,5S,6S)-4-ethoxy-3,5-dimethoxy-6-methyl-tetrahydropyran-2-ylester and{4-[1-(4-pentafluoroethyloxyphenyl)-1H-[1,2,4]triazol-3-yl]-phenyl}-carbamicacid(2R,3R,4R,5S,6S)-4-ethoxy-3,5-dimethoxy-6-methyl-tetrahydropyran-2-ylester (Compounds 201 and 202)

A solution of4-[1-(4-pentafluoroethyloxyphenyl)-1H-[1,2,4]triazol-3-yl]-phenylamine(1.0 g, 2.7 mmol) in 8 mL of dry THF was stirred while p-nitrophenylchloroformate (0.60 g, 3 mmol) was added in one portion and the solutionwas allowed to stir for 3 h. The resulting solid was filtered andair-dried, and then re-suspended in 15 mL of dry THF. The 3′-O-ethylrhamnose (0.6 g, 2.7 mmol) was added, followed by 0.12 g of 60% NaH (2.7mmol). The solution was then heated to reflux for 30 min, then anotherequivalent of NaH was added and heating resumed for another 60 min. Themixture was cooled and poured onto 50 mL of ice/water, extracted intoether, dried and concentrated. TLC shows Ca. 90:10 ratio of α- andβ-anomers, which were separated by silica gel chromatography (30%acetone in hexanes). For the α-anomer (Compound 201): ¹H NMR (CDCl₃) δ8.59 (s, 1H), 8.20 (d, J=9 Hz, 2H), 7.81 (d, J=8 Hz, 2H), 7.5 (d, J=8Hz, 2H), 7.40 (d, J=9 Hz, 2H), 6.90 (s, 1H), 6.22 (s, 1H), 3.80-3.52 (m,1H), 3.20 (t, J=9.3 Hz, 1H), 1.33 (m, 6H); EIMS 617.0 m/z (M⁺); mp192-193° C. For the β-anomer (Compound 202): ¹H NMR (CDCl₃) δ 8.59 (s,1H), 8.20 (d, J=9 Hz, 2H), 7.81 (d, J=8 Hz, 2H), 7.5 (d, J=8 Hz, 2H),7.40 (d, J=9 Hz, 2H), 7.0 (s, 1H), 5.72 (s, 1H), 3.80-3.20 (m, 12H),1.33 (m, 6H); EIMS 617.0 m/z (M⁺).

Example 76 Preparation of{4-[1-(4-pentafluoroethyloxyphenyl)-1H-[1,2,4]triazol-3-yl]-phenyl}-carbamicacid(2S,3R,4R,5S,6S)-4-propoxy-3,5-dimethoxy-6-methyl-tetrahydropyran-2-ylester (Compound 207)

A solution of4-[1-(4-pentafluoroethyloxyphenyl)-1H-[1,2,4]triazol-3-yl]-benzoyl azide(described in Example 27) (12.5 g, 29.5 mmol) in 150 mL of dry toluenewas heated at 110° C. for 90 min, then cooled to room temperature andtreated with 3-O-propyl-2,4-di-O-methyl L-rhamnose (6.9 g, 29.5 mmol)and 2.4 g of 60% NaH (60 mmol). The solution was then warmed to 40° C.for 1 h, and then it was cooled to ambient temperature and poured onto150 mL of ice/water, extracted into ether, dried and concentrated. Thecrude product was purified by silica gel chromatography and thenrecrystallized from ether-hexanes to furnish 9.6 g of Compound 207. ¹HNMR (300 MHz, CDCl₃) δ 8.58 (s, 1H), 8.2 (d, J=8 Hz, 2H), 7.82 (d, J=8Hz, 2H), 7.55 (d, J=9 Hz, 2H), 7.41 (d, J=9 Hz, 2H), 6.81 (s, 1H), 6.22(d, J=1.5 Hz, 1H), 3.75-3.44 (m, 11H), 3.23 (t, J=9.3 Hz, 1H), 1.71 (m,2H), 1.35 (d, J=6.3 Hz, 3H), 1.00 (t, J=7.5 Hz, 3H); MS 630.0 (M+H); mp158° C.

The compounds of this invention in Table 6 were prepared by the routesdescribed earlier and illustrated in Examples 71 to 76.

Example 77 Preparation of{4-[1-(4-trifluoromethoxyphenyl)-1H-imidazolyl]-phenyl}-thiocarbamicacid (2S,3R,4R,5S,6S)-3,4,5-trimethoxy-6-methyl-tetrahydropyran-2-ylester (Compound 176)

To a solution of 150 mg (0.47 mmol) of4-[1-(4-trifluoromethoxyphenyl)-1H-imidazol-4-yl]-phenylamine in 5 mL ofDCM cooled to 0° C. was added 0.09 g (0.50 mmol) ofthiocarbonyldiimidazole (TDI) and 0.07 g (0.5 mmol) ofdiisopropylethylamine (Hunig's base). After 30 min, another equivalentof TDI and Hunig's base was added, and the solution was allowed to warmto ambient temperature before concentrating and purifying bychromatography (50:50 EtOAc-hexanes) to give 0.10 g of theisothiocyanate as an off-white solid. This material was then dissolvedin 5 mL of dry THF and treated with 60 mg (0.29 mmol) of tri-O-methylrhamnose and 20 mg (0.5 mmol) of 60% NaH. The solution was allowed tostir at ambient temperature for 3 h, before it was partitioned betweenwater and EtOAc. The organic layer was then dried and concentrated.Chromatography gave 30 mg of Compound 176 as a colorless solid. ¹H NMR(300 MHz, CDCl₃) δ 7.94 (s, 1H), 7.80 (d, J=7.5 Hz, 2H), 7.50 (m, 3H),7.40 (d, J=7 Hz, 2H), 7.3 (s, 1H), 7.23 (br d, J=7 Hz, 2H), 6.80 (s,1H), 3.90-3.20 (m, 13H), 1.39 (d, J=6.3 Hz, 3H); MS 568.9 (M+H); mp 129°C.

The following thiocarbamate was also prepared by the route described inthe previous example.

Example 78 Preparation of{4-[1-(4-pentafluoroethyloxy-phenyl)-1H-[1,2,4]triazol-3-yl]-phenyl}-thiocarbamicacid(2S,3R,4R,5S,6S)-4-ethoxy-3,5-dimethoxy-6-methyl-tetrahydropyran-2-ylester (Compound 203)

¹H NMR (400 MHz, CDCl₃) δ 8.59 (s, 1H), 8.24 (d, J=7.6 Hz, 2H), 7.80 (m,4H), 7.40 (d, J=8.9 Hz, 2H), 6.79 (d, J=0.8 Hz, 1H), 3.90-3.40 (m, 10H),3.22 (m, 1H), 3.18 (t, J=9.3 Hz, 1H), 1.3 (m, 6H); MS 633.0 (M+H); mp126° C.

Example 79 Preparation of{4-[1-(4-pentafluoroethyloxy-phenyl)-1H-[1,2,4]triazol-3-yl]-phenyl}-thiocarbamicacid (2S,3R,4R,5S,6S)-3,4,5-trimethoxy-6-methyl-tetrahydropyran-2-ylester (Compound 211)

The azide prepared in Example 27 (0.22 g, 0.52 mmol) was dissolved in 5mL of toluene and heated to 110° C. for 1 h, then it was cooled andtreated with tri-O-methyl thiorhamnopyranoside (0.125 g, 0.56 mmol). Thesolution was heated to 40° C. for 1 h, then cooled, concentrated, andpurified by chromatography (0-100% EtOAc/hexanes) to afford 75 mg ofCompound 211 as a light yellow gummy solid. ¹H NMR (300 MHz, CDCl₃) δ8.58 (s, 1H), 8.18 (d, J=8.7 Hz, 2H), 7.79 (d, J=9.1 Hz, 2H), 7.53 (d,J=8.7 Hz, 2H), 7.38 (d, J=8.8 Hz, 2H), 6.78 (s, 1H), 6.23 (d, J=1.9 Hz,1H), 3.70 (m, 2H), 3.59 (s, 3H), 3.57 (s, 3H), 3.54 (s, 3H), 3.51 (m,1H), 3.21 (t, J=9.4 Hz, 1H), 1.34 (d, J=6.2 Hz, 3H).

Example 80 Preparation of{4-[1-(4-trifluoromethoxyphenyl)-1H-imidazol-4-yl]-phenyl}-thiocarbamicacid(2S,3R,4R,5S,6S)-4-ethoxy-3,5-dimethoxy-6-methyl-tetrahydropyran-2-ylester (Compound 177)

(2S,3R,4R,5S,6S)-4-Ethoxy-3,5-dimethoxy-6-methyl-tetrahydropyran-2-thiol(0.080 g, 0.34 mmol) was combined with{4-[1-(4-trifluoromethoxyphenyl)-1H-imidazol-4-yl]-phenyl}-carbamic acid4-nitrophenyl ester (0.165 g, 0.34 mmol) and Hunig's base (0.06 g, 0.46mmol) in 3 mL of THF, and the solution was heated at reflux for 2 h.Concentration and chromatography through a silica gel column thenfurnished the thiocarbamate (Compound 177) as a light yellow solid. ¹HNMR δ 7.88 (s, 1H), 7.75 (d, J=7 Hz, 2H), 7.68 (s, 1H), 7.5 (d, J=7 Hz,2H), 7.45 (s, 1H), 7.37 (d, J=8 Hz, 2H), 6.15 (d, J=1.5 Hz, 1H),3.78-3.45 (m, 11H), 3.18 (t, J=9.2 Hz, 1H), 1.36 (d, J=6.2 Hz, 3H), 1.3(t, J=7.5 Hz, 3H); mp 173-176° C.

Example 81 Preparation of4-[1-(4-trifluoromethoxyphenyl)-1H-imidazol-4-yl]-N-((2S,3R,4R,5S,6S)-3,4,5-trimethoxy-6-methyl-tetrahydropyran-2-yloxy)-benzamide(Compound 171)

A solution of 4-[1-(4-trifluoromethoxyphenyl)-1H-imidazol-4-yl]-benzoicacid (50 mg, 0.14 mmol) was treated with excess thionyl chloride andheated briefly on a steam bath. The tan oil was then concentrated invacuo and dissolved in 5 mL of THF. Compound E-30 (44 mg, 0.2 mmol) andethyldiisopropylamine (52 mg, 0.4 mmol) were added and the solution wasallowed to stir for 15 min. The solution was then partitioned betweenaqueous NaHCO₃ and ether, and the organic layer was dried, concentratedand purified by chromatography (50:50 EtOAc-hexanes) to give 20 mg ofCompound 171 as a colorless solid. ¹H NMR (400 MHz, CDCl₃) δ 7.90 (d,J=6.4 Hz, 2H), 7.89 (s, 1H), 7.80 (d, J=8.6 Hz, 2H), 7.63 (d, J=1.3 Hz,1H), 7.49 (d, J=9.3 Hz, 2H), 7.38 (d, J=8.9 Hz, 2H), 5.31 (s, 1H), 3.97(m, 1H), 3.80 (m, 1H), 3.57 (s, 3H), 3.56 (s, 3H), 3.53 (s, 3H), 3.50(m, 1H), 3.21 (t, J=9.4 Hz, 1H), 1.36 (d, J=6.2 Hz, 3H); MS 552.0 (M⁺);mp 185° C.

Example 82 Preparation of methyl{4-[1-(4-trifluoromethoxyphenyl)-1H-[1,2,4]triazol-3-yl]-phenyl}-carbamicacid(2S,3R,4R,5S,6S)-4-ethoxy-3,5-dimethoxy-6-methyl-tetrahydropyran-2-ylester (Compound 250)

Compound 193 (0.15 g, 0.26 mmol) and iodomethane were combined in 5 mLof dry DMF, and the solution was stirred under N₂ and treated with 0.025g (0.62 mmol) of NaH (60% in oil). The solution was allowed to stir atambient temperature overnight, and then it was partitioned between waterand Et₂O. Drying, concentration and chromatography of the organic layerfurnished 73 mg of Compound 250 as a colorless solid foam. ¹H NMR (300MHz, CDCl₃) δ 8.61 (s, 1H), 8.2 (d, J=8 Hz, 2H), 7.82 (d, J=8 Hz, 2H),7.55 (d, J=9 Hz, 2H), 7.41 (d, J=9 Hz, 2H), 6.17 (s, 1H), 3.7-3.4 (m,11H), 3.39 (s, 3H, N—CH₃), 3.18 (t, J=9 Hz, 1H), 1.35 (d, J=6.3 Hz, 3H),1.2 (t, J=7 Hz, 3H); MS 581.9 ([M+H]⁺).

Example 83 Preparation of methyl{4-[1-(4-pentafluoroethoxy-phenyl)-1H-[1,2,4]triazol-3-yl]-phenyl}-carbamicacid(2S,3R,4R,5S,6S)-4-ethoxy-3,5-dimethoxy-6-methyl-tetrahydropyran-2-ylester (Compound 251)

Compound 207 was methylated as in Example 82 to give Compound 251. ¹HNMR (300 MHz, CDCl₃) δ 8.60 (s, 1H), 8.20 (d, J=68 Hz, 2H), 7.83 (d,J=8.8 Hz, 2H), 7.41 (d, J=9 Hz, 2H), 7.39 (d, J=8.6 Hz, 2H), 6.17 (s,1H), 3.70-3.40 (m, 11H), 3.39 (s, 3H, NCH₃), 1.38 (d, J=6.0 Hz, 3H),1.20 (t, J=7.5 Hz, 3H); MS 630.99 ([M+H]⁺).

Example 84 Preparation ofmethyl-{4-[1-(4-pentafluoroethyloxy-phenyl)-4,5-dihydro-1H-pyrazol-4-yl]-phenyl}-carbamicacid(2S,3R,4R,5S,6S)-4-ethoxy-3,5-dimethoxy-6-methyl-tetrahydropyran-2-ylester (Compound 252)

Compound 179 was methylated as in Example 82 to give Compound 252. ¹HNMR (300 MHz, CDCl₃) δ 7.68 (d, J=8.24 Hz, 2H), 7.24 (d, J=8.24 Hz, 2H),7.12 (d, J=8.28 Hz, 2H), 7.08 (d, J=8.28 Hz, 2H), 6.12 (d, J=1.85 Hz,1H), 3.92 (t, J=9.44 Hz, 2H), 3.79-3.61 (m, 4H), 3.57 (s, 3H), 3.56 (s,3H), 3.44 (dd, J=9.31, 3.36 Hz, 1H), 3.38 (s, 3H), 3.32-3.18 (m, 3H),1.36-1.23 (m, 6H); EI/MS 631 (M⁺).

Example 85 Preparation of ethyl{4-[1-(4-pentafluoroethoxy-phenyl)-1H-[1,2,4]triazol-3-yl]-phenyl}-carbamicacid(2S,3R,4R,5S,6S)-4-propoxy-3,5-dimethoxy-6-methyl-tetrahydropyran-2-ylester (Compound 253)

Compound 207 was N-ethylated as in Example 82, using iodoethane insteadof iodomethane, to give Compound 253. ¹H NMR (300 MHz, CDCl₃) δ 8.60 (s,1H), 8.22 (d, J=68 Hz, 2H), 7.83 (d, J=8.8 Hz, 2H), 7.41 (d, J=9 Hz,2H), 7.39 (d, J=8.6 Hz, 2H), 6.17 (s, 1H), 3.8 (q, J=7.5 Hz, 2H),3.60-3.30 (m, 11H), 3.10 (br s, 1H), 1.38 (d, J=6.0 Hz, 3H), 1.20 (t,J=7.5 Hz, 3H); MS 659.12 ([M+H]⁺).

Example 86 Preparation of methoxymethyl{4-[1-(4-trifluoromethoxyphenyl)-1H-[1,2,4]triazol-3-yl]-phenyl}-carbamicacid(2S,3R,4R,5S,6S)-4-ethoxy-3,5-dimethoxy-6-methyl-tetrahydropyran-2-ylester (Compound 254)

Compound 193 (0.15 g, 0.26 mmol) and bromomethyl methyl ether (78 mg,0.6 mmol) were combined in 5 mL of dry THF, and the solution was stirredunder N2 and treated with 0.025 g (0.6 mmol) of NaH (60% in oil). Thesolution was allowed to stir at ambient temperature overnight, and thenit was partitioned between water and Et₂O. Drying, concentration andchromatography of the organic layer furnished 110 mg of Compound 254 asa colorless solid foam. ¹H NMR (300 MHz, CDCl₃) δ 8.61 (s, 1H), 8.24 (d,J=8 Hz, 2H), 7.82 (d, J=8 Hz, 2H), 7.4 (overlapping d, J=8 Hz, 4H), 6.17(s, 1H), 5.05 (br s, 2H), 3.6-3.3 (m, 14H), 3.18 (t, J=9 Hz, 1H), 1.35(d, J=6.3 Hz, 3H), 1.2 (t, J=7 Hz, 3H); MS 611.8 ([M+H]⁺).

Example 87 Preparation of methoxymethyl{4-[1-(4-pentafluoroethoxyphenyl)-1H-[1,2,4]triazol-3-yl]-phenyl}-carbamicacid

(2S,3R,4R,5S,6S)-4-ethoxy-3,5-dimethoxy-6-methyl-tetrahydropyran-2-ylester (Compound 255).

Methoxymethylation of Compound 201, using conditions described inExample 86, gave Compound 255 as a viscous foam. ¹H NMR (300 MHz, CDCl₃)δ 8.61 (s, 1H), 8.22 (d, J=8 Hz, 2H), 7.82 (d, J=8 Hz, 2H), 7.4 (m, 4H),6.17 (s, 1H), 5.05 (br s, 2H), 3.6-3.3 (m, 14H), 3.18 (t, J=9 Hz, 1H),1.35 (d, J=6.3 Hz, 3H), 1.2 (t, J=7 Hz, 3H); MS 661.8 ([M+H]⁺).

Example 88 Preparation of allyl{4-[1-(4-pentafluoroethoxy-phenyl)-1H-[1,2,4]triazol-3-yl]-phenyl}-carbamicacid(2S,3R,4R,5S,6S)-4-ethoxy-3,5-dimethoxy-6-methyl-tetrahydropyran-2-ylester (Compound 256)

60% NaH (0.015 g, 0.40 mmol) was added to a solution of Compound 201(0.15 g, 0.24 mmol) and allyl bromide (0.41 g, 0.34 mmol) in dry DMF(1.1 mL) at 0° C. under N₂. The reaction mixture was then allowed towarm to 25° C. and stirred for 5 h, at which point it was poured ontoice-H₂O (50 mL) and was extracted with EtOAc (3×50 mL). The combinedorganic extracts were washed with H₂O (50 mL) and were dried (Na₂SO₄),filtered and concentrated. Chromatography afforded Compound 256 (0.040g, 25%) as a white gummy solid. ¹H NMR (300 MHz, CDCl₃) δ 8.59 (s, 1H),8.21 (d, J=8.1 Hz, 2H), 7.83 (d, J=9.0 Hz, 2H), 7.42 (d, J=9.3 Hz, 2H),7.35 (br, 2H), 6.17 (br, 1H), 6.00-5.92 (m, 1H), 5.27-5.17 (m, 2H), 4.34(br, 2H), 3.80-3.30 (m, 11H), 3.08 (br, 1H), 1.44 (br, 3H), 1.30 (br,3H); MS 657 ([M]⁺).

Example 89 Preparation of hydroxymethyl{4-[1-(4-pentafluoroethoxy-phenyl)-1H-[1,2,4]triazol-3-yl]-phenyl}-carbamicacid(2S,3R,4R,5S,6S)-4-propoxy-3,5-dimethoxy-6-methyl-tetrahydropyran-2-ylester (Compound 257)

A solution of Compound 207 (0.15 g, 0.24 mmol) was dissolved in 4 mL ofDCM and treated with paraformaldehyde (50 mg, excess) andtrifluoroacetic acid (250 μL, excess). The solution was stirred atambient temperature for 20 h, and then it was concentrated in vacuo.Chromatography (0 to 100% EtOAc in hexanes) gave 25 mg of thehydroxymethyl derivative (Compound 257) as a solid foam. ¹H NMR (300MHz, CDCl₃) δ 8.60 (s, 1H), 8.20 (d, J=68 Hz, 2H), 7.83 (d, J=8.8 Hz,2H), 7.41 (d, J=9 Hz, 4H), 7.39 6.17 (s, 1H), 5.15 (dd, J=6, 14 Hz, 2H),3.65-3.20 (m, 12H), 3.15 (br s, 1H), 1.52 (m, 2H), 1.38 (d, J=6.0 Hz, 3H0.95 (t, J=7.5 Hz, 3H); MS 661.10 ([M+H]⁺).

Example 90 Preparation of acetyl{4-[1-(4-pentafluoroethoxyphenyl)-1H-[1,2,4]triazol-3-yl]-phenyl}-carbamicacid(2S,3R,4R,5S,6S)-4-ethoxy-3,5-dimethoxy-6-methyl-tetrahydropyran-2-ylester (Compound 258)

60% NaH (0.016 g, 0.40 mmol) was added to a solution of Compound 201(0.15 g, 0.24 mmol) in dry DMF (1.1 mL) at 0° C. under N₂ and themixture was stirred for ˜5 min. Acetyl chloride (0.03 mL, 0.42 mmol) wasthen added, and the reaction mixture was allowed to warm to 25° C. andstirred for a total of 64 h. The mixture was poured onto ice-H₂O (50 mL)and was extracted with EtOAc (3×50 mL). The combined organic extractswere washed with H₂O (50 mL) and satd aq NaCl (75 mL) and were dried(Na₂SO₄), filtered and concentrated. Chromatography afforded Compound258 (0.042 g, 26%) as a light yellow solid. ¹H NMR (400 MHz, CDCl₃) δ8.59 (s, 1H), 8.29 (d, J=8.1 Hz, 2H), 7.81 (d, J=9.0 Hz, 2H), 7.40 (d,J=9.1 Hz, 2H), 7.24 (d, J=8.5 Hz, 2H), 6.07 (d, J=2.0 Hz, 1H), 3.48 (s,3H), 3.41 (s, 3H), 3.49-3.35 (m, 1H), 3.31-3.20 (m, 3H), 3.04 (t, J=9.4Hz, 1H), 2.74 (dd, J=9.8, 3.4 Hz, 1H), 2.69 (s, 3H), 1.25 (d, J=6.1 Hz,3H), 1.01 (t, J=7.0 Hz, 3H); MS 658 (M⁺); mp 70-72° C.

Example 91 Preparation of4-(((2S,3R,4R,5S,6S)-4-ethoxy-3,5-dimethoxy-6-methyl-tetrahydropyran-2-yloxycarbonyl)-{4-[1-(4-pentafluoroethoxy-phenyl)-1H-[1,2,4]triazol-3-yl]-phenyl}-amino)-4-oxo-butyricacid methyl ester (Compound 259)

60% NaH (0.041 g, 1.0 mmol) was added in one portion to a solution ofCompound 201 (0.500 g, 0.81 mmol) in dry DMF (3.6 mL) at 25° C. and themixture was stirred for ˜5 min. Methyl succinyl chloride (0.12 mL, 0.97mmol) was then added, and the reaction mixture was allowed to stir at60° C. for 3 h. The mixture was cooled, poured onto satd aq NH₄Cl (50mL) and was extracted with EtOAc (3×50 mL). The combined organicextracts were washed with H₂O (50 mL) and satd aq NaCl (75 mL) and weredried (Na₂SO₄), filtered and concentrated. Chromatography affordedCompound 259 (0.079 g, 13%) as a white solid. ¹H NMR (300 MHz, CDCl₃) δ8.60 (s, 1H), 8.30 (d, J=9.0 Hz, 2H), 7.82 (d, J=9.0 Hz, 2H), 7.41 (d,J=8.7 Hz, 2H), 7.29-7.22 (m, 2H), 6.08 (d, J=1.8 Hz, 1H), 3.70 (s, 3H),3.50-3.19 (m, 9H), 3.05 (t, J=9.3 Hz, 1H), 2.79-2.69 (m, 3H), 1.29-1.22(m, 6H), 1.03 (t, J=6.9 Hz, 3H); MS 730 (M⁺); mp 72-76° C.

Testing of Compounds

Bioassays on beet armyworm (BAW; Spodoptera exigua: Lepidoptera) wereconducted using either a 96-well microtiter plate-based high throughput(HTS) bioassay or a 128-well diet tray assay. The HTS assay is a basedon a modification of Lewer et al. J. Nat. Prod. 2006, 69, 1506. BAW eggsof were placed on top of artificial diet (100 μl) in each well of96-well microtiter plate. The diet was pretreated with test compounds(12 μg dissolved in 30 μL of DMSO-acetone-water mixture) layered on topof the diet using a liquid handling system and then allowed to dry forseveral hours. Infested plates were then covered with a layer of sterilecotton batting and the plate lid, and then held in the dark at 29° C.Mortality was recoded at 6 d post-treatment. Each plate had sixreplicates. The percent mortality was calculated from the average of thesix replicates. In the case of the 128-well diet assay, three to fivesecond instar BAW larvae were placed in each well (3 mL) of the diettray that had been previously filled with 1 mL of artificial diet towhich 50 μg/cm² of the test compound (dissolved in 50 μL of 90:10acetone-water mixture) had been applied (to each of eight wells) andthen allowed to dry. Trays were covered with a clear self-adhesivecover, and held at 25° C., 14:10 light-dark for six days. Percentmortality was recorded for the larvae in each well; activity in theeight wells was then averaged. The results for both bioassays areindicated in Table 7. In Table 7, under the BAW HTS or BAW 50 heading,an “A” means that the compound was tested and at least 50 percentmortality was observed whereas, “B” means that either (1) the compoundwas tested and less than 50 percent mortality was observed or (2) thecompound was not tested.

TABLE 1

# A R1 R2 R3 R4 Sugar M.S. bp ¹H NMR (CDCl₃, δ) E-1  OCH₃ OCH₃ OCH₃ OCH₃CH₃ L-rhamnose — 150° C. 5.28 (m, 1 H), 3.85 (m, 1 H), 3.66 (m, 1 H),3.60- (0.5 mm 3.50 (m, 1 H), 3.58 (s, 3 H), 3.53 (s, 6 H), 3.37 (s, Hg)3 H), 3.16 (t, 1 H), 1.31 (d, 3 H) E-2  OH OCH₃ OCH₃ OCH₃ CH₃ L-rhamnose— 145-155° C. 5.28 (s, 1 H), 3.83 (m, 1 H), 3.7-3.45 (m, 11 H), 3.16 (1mm (t, J = 9.2 Hz, 1 H), 3.0 (s, 1 H), 1.31 (d, J = 6 Hz, Hg) 3 H) E-3 OCH₃ OCH₃ OC₂H₅ OCH₃ CH₃ L-rhamnose 202.9 165° C. 4.71 (d, J = 1.8 Hz, 1H), 3.77-3.50 (m, 11 H), 3.37 (M- (10 (s, 3 H), 3.13 (t, J = 9.4 Hz, 1H), 1.32 (d, J = 6.3 MeOH) mTorr) Hz, 3 H), 1.27 (t, J = 7.0 Hz, 3 H)E-4  OC₂H₅ OC₂H₅ OC₂H₅ OC₂H₅ CH₃ L-rhamnose 299.1 180° C. 4.72 (d, J =1.8 Hz) and 4.30 (s), total 1 H, 4.0-3.35 (M + Na) (10 (series of m, 10H), 3.2 (m, 2 H), 1.3-1.1 (m, 15 H) mTorr) E-5  OCH₃ OCH₃ OC₃H₇ OCH₃ CH₃L-rhamnose 175° C. 4.70 (d, J = 1.8 Hz, 1 H), 3.77-3.50 (m, 11 H), 3.37(10 (s, 3 H), 3.13 (t, J = 9.4 Hz, 1 H), 1.62 (m, 2 H), mTorr) 1.32 (d,J = 6.3 Hz, 3 H), 0.98 (t, J = 7.5 Hz, 3 H) E-6  OCH₃ OCH₃ O-allyl OCH₃CH₃ L-rhamnose 175° C. 5.98 (m, 1 H), 5.32 (d, 1 H), 5.20 (d, 1 H), 4.50(s, (10 1 H), 4.18 (d, 2 H), 3.62-3.50 (m, 9 H), 3.28 (s, 3 H), mTorr)3.17 (t, J = 6.3 Hz, 1 H), 1.33 (d, J = 6.3 Hz, 3 H) E-7  OCH₃ OCH₃OC₄H₉ OCH₃ CH₃ L-rhamnose 165° C. 4.71 (s, 1 H), 3.62-3.50 (m, 11 H),3.35 (s, 3 H), (5 3.17 (t, 1 H), 1.6 (m, 2 H), 1.4 (m, 2 H), 1.33 (d, J= mTorr) 6.3 Hz, 3 H), 0.98 (t, J = 7.5 Hz, 3 H) E-8  OH OCH₃ OC₂H₅ OCH₃CH₃ L-rhamnose 202.9 165° C. 5.35 (m, J = 3.2, 2.0 Hz, 1 H), 3.84-3.62(m, 5 H), (M + H₂O) (9 3.59 (s, 3 H), 3.53 (s, 3 H), 3.16 (t, J = 9.5Hz, 1 H), mTorr) 2.73 (d, J = 3.4 Hz, 1 H), 1.33-1.26 (m, 6 H) E-9  OHOC₂H₅ OC₂H₅ OC₂H₅ CH₃ L-rhamnose 248.2 203° C. 5.2 (s) and 4.65 (dd, J =1.2, 9 Hz, anomeric (M+) (5 proton signals, total 1 H, ratio 64:36 α:β);4.10- mTorr) 3.45 (m, 8 H), 3.36-3.20 (m, 2 H), 1.37-1.13 (m, 12 H) E-10OH OCH₃ OC₃H₇ OCH₃ CH₃ L-rhamnose 220.2 185° C. 5.25 (dd, J = 3.2, 2.0Hz) and 4.61 (m, total 1 H), (M+) (5 3.80 (m, 1 H), 3.70-3.50 (m, 9 H),3.36-3.05 (m, mTorr) 1 H), 1.60 (m, 2 H), 1.30 (m, 5 H), 0.95 (t, J =7.5 Hz, 3 H) E-11 OH OCH₃ O-allyl OCH₃ CH₃ L-rhamnose 254.9 175° C. 5.95(m, 1 H), 5.3 (m, 1 H), 5.19 (m, 1 H), 5.21 and (M + Na) (10 4.61 (bothm, α and β anomers, total 1 H), 4.20 (m, mTorr) 2 H), 3.80 (m, 1 H),3.70-3.50 (m, 7 H), 3.40-3.10 (m, 3 H), 1.3 (m, 3 H) E-12 OH OCH₃ OC₄H₉OCH₃ CH₃ L-rhamnose 248.2 189° C. 5.35 (dd, J = 3.2, 2.0 Hz) and 4.45(m, total 1 H), (M+) (5 3.80 (m, 1 H), 3.70-3.50 (m, 10 H), 3.36-3.05(m, mTorr) 1 H), 2.73 (d, J = 3.4 Hz, 1 H), 1.60 (m, 2 H), 1.40 (m, 2H), 1.33 (d, J = 6 Hz, 3 H), 0.95 (t, J = 7.5 Hz, 3 H) E-13 —OH —OCH₃—OCH₃ —OCH₃ CH₂O— L-mannose 5.32 (s, 1 H), 3.9 (m, 1 H), 3.66-3.53(series of m, CH₃ 4 H) 3.52 (s, 3 H), 3.51 (s, 3 H), 3.49 (s, 3 H), 3.40(s, 3 H), 3.35 (m, 1 H), 3.18 (d, J = 3 Hz, 1 H) E-14 —OH —OCH₃ —OCH₃—OCH₃ CH₂O— D-glucose 5.33 (d, J = 3.6 Hz) and 4.60 (d, J = 4 Hz), α andβ CH₃ anomers, total 1 H), 3.9 (m, 1 H), 3.6-3.3 (series of s and m, 14H), 3.28 (m, 3 H), 1.7 (s, 1 H) E-15 —OCH₃ —OCH₃ —OCH₃ —OCH₃ —H₂L-xylose 207 4.77 (d, J = 3.5 Hz) and 4.15 (d, J = 7.4 Hz, total (M + H)1 H in a 0.27:1 α:β ratio), 4.00 (dd, J = 11.6, 5.0 Hz, 1 H), 4.03-2.93(series of s and m, 16 H) E-16 —OH —OCH₃ —OCH₃ —OCH₃ —H₂ L-xylose 1755.23 (t, J = 3.4 Hz) and 4.60 (t, J = 6.3 Hz, total (M − H₂O) 1 H in a1.5:1 α:β ratio), 4.01-2.97 (series of s and m, 15 H) E-17 —OCH₃ —OCH₃—OCH₃ —OCH₃ —H₂ L-lyxose 207 4.69 (d, J = 3.0 Hz, 1 H, α anomer), 3.77(dd, J = (M + H) 10.8, 4.7 Hz, 1 H), 3.62-3.32 (series of s and m, 1 6H) E-18 —OH —OCH₃ —OCH₃ —OCH₃ —H₂ L-lyxose 175 5.18-5.11 (m, 1 H,mixture of α and β anomers), (M − H₂O) 4.84 (d, J = 10.1 Hz, 0.4 H),3.98-3.37 (series of s and m, 14 H), 3.11 (d, J = 4.2 Hz, 0.6 H) E-19—OCH₃ —OCH₃ —OCH₃ —OCH₃ CH₂O— L-glucose 205 (600 MHz, CDCl₃) 4.83 (d, J= 4.1 Hz) and 4.14 CH₃ (M − (d, J = 7.8 Hz, total 1 H in a 0.2:1 α:βratio), 3.66- CH₂OCH₃) 3.36 (series of s and m, 18 H), 3.29-3.26 (m, 1H), 3.17-3.13 (m, 1 H), 3.01-2.94 (m, 1 H) E-20 —OH —OCH₃ —OCH₃ —OCH₃CH₂O— L-glucose 191 Mp 63- 5.33 (d, J = 3.7 Hz) and 4.58 (d, J = 7.9 Hz,total CH₃ (M − 67° C. 1 H in a 2.5:1 α:β ratio), 3.92-3.86 (m, 0.8 H),3.65- CH₂OCH₃) 3.08 (series of s and m, 18 H), 2.96 (dd, J = 8.8, 7.8Hz, 0.2 H) E-21 —OCH₃ —H₂ —OCH₃ —OCH₃ CH₂O— 2-deoxy-D- 220 (M⁺) 4.81(dd, J = 3.6, 1.1 Hz) and 4.34 (dd, J = 9.5, 1.9 CH₃ glucose Hz, total 1H in a 0.29:1 α:β ratio), 3.71-3.23 (m, 16 H), 3.18-3.05 (m, 1 H),2.33-2.16 (m, 1 H), 1.60- 1.41 (m, 1 H) E-22 —OCH₃ —H₂ —OCH₃ OH CH₃ L-4.78 (d, J = 3.3 Hz, 1 H), 3.52 (m, 1 H), 3.47 (m, oleandrose 1 H), 3.45(s, 3 H), 3.30 (s, 3 H), 3.19 (m, 1 H), 2.67 (brs, 1 H), 2.29 (dd, J =4.8, 12.9 Hz, 1 H), 1.51 (m, 1 H), 1.32 (d, J = 6.3 Hz, 3 H)

TABLE 2

# R1 R2 R3 R4 Sugar M.S. mp ¹H NMR (CDCl₃, δ) E-23 OCH₃ OCH₃ OCH₃ CH₃ L-326.1 135° C. 5.35 (d, J = 2.0 Hz, 1 H), 4.29 (m, 1 H), 3.89 (dd, J =rhamnose [M + Na]⁺ 3.3, 2.1 Hz, 1 H), 3.55 (s, 3 H), 3.54 (s, 3 H), 3.52(s, 3 H), 3.51 (m, 1 H), 3.18 (t, J = 9.3 Hz, 1 H), 2.74 (s, 4 H), 1.27(d, J = 6.1 Hz, 3 H) E-24 OCH₃ OCH₃ OH CH₃ L- 288 163- 5.42 (s, 1 H),4.40 (m, 1 H), 4.0 (m, 1 H), 3.63 (d, J = 8 rhamnose [M − H] 166° C. Hz,1 H), 3.55-3.45 (m, 7 H), 2.78 (s, 4 H), 2.2 (br s, 1 H), 1.30 (d, J =6.3 Hz, 3 H) E-25 OCH₃ OC₂H₅ OCH₃ CH₃ L- 5.35 m, 1 H), 4.29 (m, 1 H),3.85 (m, 1 H), 3.78-3.50 (m, rhamnose 9 H), 3.19 (t, J = 9.5 Hz, 1 H),2.75 (s, 4 H), 1.33-1.26 (m, 6 H) E-26 OCH₃ OC₃H₇ OCH₃ CH₃ L- 354. 69-5.35 (s, 1 H), 4.29 (m, 1 H), 3.84 (m, 1 H), 3.78-3.50 (m, rhamnose [M +Na]⁺ 71° C. 9 H), 3.19 (t, J = 9.5 Hz, 1 H), 2.75 (s, 4 H), 1.64 (m, 2H), 1.25 (d, J = 6.1 Hz, 3 H), 0.95 (t, J = 7.5 Hz, 3 H)) E-27 OCH₃OC₄H₉ OCH₃ CH₃ L- 5.32 (d, J = 1.8 Hz, 1 H), 4.29 (m, 1 H), 3.84 (m, 1H), rhamnose 3.6-3.45 (m, 9 H), 3.17 (t, J = 9.3 Hz, 1 H), 2.73 (s, 4H), 1.6 (m, 2 H), 1.4 (m, 2 H), 1.26 (d, J = 5.7 Hz, 3 H), 0.93 (t, J =7.5 Hz, 3 H) E-28 OCH₃ OCH₃ OCH₃ CH₂OCH₃ D-glucose 5.52 (d, J = 4 Hz, 1H), 4.45 (d, J = 10 Hz, 1 H), 3.68- 3.47 (m, 12 H), 3.4-3.27, series ofm, 5 H), 2.72 (s, 4 H) E-29 OCH₃ OCH₃ OCH₃ CH₂OCH₃ L- 5.44 (s, 1 H),4.29 (m, 1 H), 3.90 (m, 1 H), 3.7-3.55 (m, 3 mannose H), 3.54 (s, 3 H),3.53 (s, 3 H), 3.52 (s, 3 H), 3.53 (m, 1 H), 3.38 (s, 3 H), 2.73 (s, 4H)

TABLE 3

# R1 R2 R3 R4 Sugar M.S. Mp ¹H NMR (CDCl₃, δ) E-30 OCH₃ OCH₃ OCH₃ CH₃ L-221.7 55° C. 5.51 (s, 2 H), 4.98 (d, J = 1.8 Hz, 1 H), 3.60 (m, rhamnose(M + H⁺) 2 H), 3.55 (s, 3 H), 3.50 (s, 3 H), 3.48 (s, 3 H), 3.35 (dd, J= 9.2, 3.3 Hz, 1 H), 3.13 (t, J = 9.4 Hz, 1 H), 1.34 (d, J = 6.2 Hz, 3H) E-31 OCH₃ OC₂H₅ OCH₃ CH₃ L- 258.1 88° C. 5.51 (s, 2 H), 4.98 (d, J =1.8 Hz, 1 H), 3.60 (m, rhamnose (M + Na⁺) 4 H), 3.55 3.50 (s, 3 H), 3.48(s, 3 H), 3.35 (dd, J = 9.2, 3.3 Hz, 1 H), 3.13 (t, J = 9.4 Hz, 1 H),1.34- 1.26 (m, 6 H) E-32 OCH₃ OC₃H₇ OCH₃ CH₃ L- 249.1 49° C. 5.6 (s, 2H), 4.95 (d, J = 1.8 Hz, 1 H), 3.6-3.3 (m, rhamnose (M + H⁺) 11 H), 3.13(t, J = 9.3 Hz, 1 H), 1.65 (m, 2 H), 1.34 (d, J = 6.2 Hz, 3 H), 0.97 (t,J = 7.5 Hz, 3 H) E-33 OCH₃ OC₄H₉ OCH₃ CH₃ L- 40- 5.6 (s, 2 H), 4.97 (d,J = 1.8 Hz, 1 H), 3.6-3.3 (m, rhamnose 42° C. 11 H), 3.13 (t, J = 9.3Hz, 1 H), 1.62 (m, 2 H), 1.40 (m, 2 H), 1.34 (d, J = 6.2 Hz, 3 H), 0.94(t, J = 7.5 Hz, 3 H) E-34 OC₂H₅ OC₂H₅ OC₂H₅ CH₃ L- 264.1 Oil 5.5 (s, 2H), 4.90 (s, 1 H), 3.9 (m, 1 H), 3.80-3.50 rhamnose (M + Na⁺) (m, 7 H),3.4 (m, 1 H), 3.25 (t, J = 9 Hz, 1 H), 1.35 (d, J = 6.3 Hz, 3 H), 1.27(m, 9 H) E-35 OCH₃ OCH₃ OH CH₃ L- 268 Oil 5.6 (br s, 2 H), 4.96 (s, 1H), 3.7-3.5 (m, 3 H), 3.48 rhamnose (M + (s, 3 H), 3.42 (s, 3 H), 3.25(dd, J = 10, 3 Hz, 1 H), AcOH) 2.75 (br s, 1 H), 1.7 (d, J = 7 Hz, 3 H)E-36 OCH₃ OCH₃ OCH₃ CH₂OCH₃ L-mannose 251.1 58° C. 5.5 (br s, 2 H), 5.04(d, J = 2 Hz, 1 H), 3.65-3.58 (M + H⁺) (m, 4 H), 3.52 (s, 3 H), 3.48(two s, 6 H), 3.42 (s, 3 H), 3.45-3.39 (m, 2 H). E-37 OCH₃ OCH₃ OCH₃ CH₃L-fucose 91° C. 5.58 (s, 2 H), 5.1 (d, J = 4 Hz, 1 H), 3.60 (q, J = 6.8Hz, 1 H), 3.66 (m, 1 H), 3.60 (s, 3 H), 3.53 (s, 3 H), 3.51 (s, 3 H),3.5-3.4 (m, 2 H), 1.34 (d, J = 6.4 Hz, 3 H) E-38 OCH₃ OCH₃ OCH₃ CH₂OCH₃D-glucose 251.8 82° C. 5.6 (br. s, 2 H), 5.1 (d, J = 4 Hz, 1 H), 3.7 (s,3 H), (M + H)⁺ 3.55 (s, 3 H), 3.53 (s, 3 H), 3.41 (s, 3 H), 3.65-3.35(series of m, 3 H), 3.4 (m, 1 H), 3.2 (m, 2 H)

TABLE 4

Het Mp ¹H NMR # Ar₁ link¹ Het Ar₂ Sugar² M.S. ° C. (CDCl₃, δ)³ 1 3-OCH₃4,1 pyrazole 1,4 A 481.0 8.22 (d, J = 8.24 Hz, 2 H), 8.06 (s, 1 H),7.82-7.78 (m, 5 H), 7.39-7.36 (m, 1 H), 7.21-7.17 (m, phenyl Phenyl [M]⁺1 H), 6.87 (m, 1 H), 5.63 (d, J = 1.85 Hz, 1 H), 3.84 (s, 3 H), 3.68(dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1 H), 3.20 (t, J = 9.48Hz, 1 H), 1.25 (d, J = 6.26 Hz, 3 H) 2 4-Cl 3,1 pyrazole 1,4 A 485.08.18 (s, 1 H), 8.02 (d, J = 2.01 Hz, 1 H), 7.81 (d, J = 8.32 Hz, 2 H),7.78 (d, J = 8.32 Hz, 2 H), phenyl Phenyl [M + H]⁺ 7.47 (d, J = 8.22 Hz,2 H), 7.29 (d, J = 8.22 Hz, 2 H), 7.01 (d, J = 2.01 Hz, 1 H), 5.63 (d, J= 1.85 Hz, 1 H), 3.68 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59(s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1H), 3.20 (t, J = 9.48 Hz, 1 H), 1.25 (d, J = 6.26 Hz, 3 H) 3 2-pyridyl3,1 pyrazole 1,4 A 452.0 8.64 (m, 1 H), 8.19 (s, 1 H), 8.16-8.11 (m, 1H), 8.04 (d, J = 1.98 Hz, 1 H), 7.81 (d, J = 8.34 Hz, Phenyl [M]⁺ 2 H),7.78-7.69 (m, 4 H), 7.13 (d, J = 1.98 Hz, 1 H), 5.63 (d, J = 1.85 Hz, 1H), 3.68 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3 H),3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1 H), 3.20(t, J = 9.48 Hz, 1 H), 1.25 (d, J = 6.26 Hz, 3 H) 4 2-thienyl 3,1pyrazole 1,4 A 457.0 8.16 (s, 1 H), 7.94 (d, J = 1.91 Hz, 1 H), 7.79 (d,J = 8.30 Hz, 2 H), 7.69 (d, J = 8.30 Hz, 2 H), Phenyl [M]⁺ 7.42 (m, 1H), 7.31 (m, 1 H), 7.07 (m, 1 H), 6.68 (d, J = 1.91 Hz, 1 H), 5.63 (d, J= 1.85 Hz, 1 H), 3.68 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59(s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1H), 3.20 (t, J = 9.48 Hz, 1 H), 1.25 (d, J = 6.26 Hz, 3 H) 5 4-(1-OH-1,3 pyrazole 1,4 A 509.0 8.17 (s, 1 H), 7.96 (d, J =3.34 Hz, 1 H), 7.92(d, J = 8.23 Hz, 2 H), 7.74 (d, J = 8.30 Hz, 2 H), propyl) Phenyl [M]⁺7.66 (d, J = 8.23 Hz, 2 H), 7.42 (d, J = 8.30 Hz, 2 H), 6.79 (d, J =3.34 Hz, 1 H), 5.63 (d, J = phenyl 1.85 Hz, 1 H), 4.62 (t, J = 7.26 Hz,1 H), 3.73 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3 H),3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1 H), 3.18(t, J = 9.48 Hz, 1 H), 1.79 (m, 3 H), 1.31 (d, J = 6.26 Hz, 3 H), 0.94(t, J = 7.40, 3 H) 6 4-SCF₃ 1,3 pyrazole 1,4 A 551.0 8.18 (s, 1 H), 7.99(d, J = 3.32 Hz, 1 H), 7.94 (d, J = 8.22 Hz, 2 H), 7.82 (d, J = 8.29 Hz,2 H), phenyl Phenyl [M + H]⁺ 7.74 (d, J = 8.29 Hz, 2 H), 7.68 (d, J =8.22 Hz, 2 H), 6.83 (d, J = 3.32 Hz, 1 H), 5.63 (d, J = 1.85 Hz, 1 H),3.72 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3 H), 3.57(s, 3 H), 3.56 (s, 3 H), 3.42 (dd, J = 9.31, 3.36 Hz, 1 H), 3.20 (t, J =9.48 Hz, 1 H), 1.28 (d, J = 6.26 Hz, 3 H) 7 4-OC₂F₄H 1,3 pyrazole 1,4 A567.0 8.18 (s, 1 H), 7.97 (d, J = 3.22 Hz, 1 H), 7.91 (d, J = 8.28 Hz, 2H), 7.78 (d, J = 8.31 Hz, 2 H), phenyl Phenyl [M + H]⁺ 7.69 (d, J = 8.28Hz, 2 H), 7.31 (d, J = 8.31 Hz, 2 H), 6.81 (d, J = 3.22 Hz, 1 H), 5.94(tt, J = 52.72, 2.64 Hz, 1 H), 5.63 (d, J = 1.85 Hz, 1 H), 3.77 (dd, J =3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.56(s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1 H), 3.18 (t, J = 9.48 Hz, 1 H),1.31 (d, J = 6.26 Hz, 3 H) 8 4-OC₂F₅ 1,3 pyrazole 1,4 A 585.0 8.17 (s, 1H), 7.95 (d, J = 3.30 Hz, 1 H), 7.91 (d, J = 8.21 Hz, 2 H), 7.79 (d, J =8.29 Hz, 2 H), phenyl Phenyl [M + H]⁺ 7.70 (d, J = 8.21 Hz, 2 H), 7.31(d, J = 8.29 Hz, 2 H), 6.81 (d, J = 3.30 Hz, 1 H), 5.63 (d, J = 1.85 Hz,1 H), 3.74 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3 H),3.57 (s, 3 H), 3.56 (s, 3 H), 3.41 (dd, J = 9.31, 3.36 Hz, 1 H), 3.19(t, J = 9.48 Hz, 1 H), 1.32 (d, J = 6.26 Hz, 3 H) 9 4-SCH₃ 1,3 pyrazole1,4 A 497.0 8.18 (s, 1 H), 7.94 (d, J = 3.36 Hz, 1 H), 7.91 (d, J = 8.21Hz, 2 H), 7.71 (d, J = 8.20 Hz, 2 H), phenyl Phenyl [M + H]⁺ 7.69 (d, J= 8.21 Hz, 2 H), 7.36 (d, J = 8.20 Hz, 2 H), 6.78 (d, J = 3.36 Hz, 1 H),5.63 (d, J = 1.85 Hz, 1 H), 3.72 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m,1 H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31,3.36 Hz, 1 H), 3.20 (t, J = 9.48 Hz, 1 H), 2.52 (s, 3 H), 1.28 (d, J =6.26 Hz, 3 H) 10 4-i-Pr 1,3 pyrazole 1,4 A 493.0 8.18 (s, 1 H), 7.93 (d,J = 8.25 Hz, 2 H), 7.90 (d, J = 3.34 Hz, 1 H), 7.69 (d, J = 8.29 Hz, 2H), phenyl Phenyl [M + H]⁺ 7.66 (d, J = 8.25 Hz, 2 H), 7.33 (d, J = 8.29Hz, 2 H), 6.78 (d, J = 3.34 Hz, 1 H), 5.63 (d, J = 1.85 Hz, 1 H), 3.79(dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1 H), 3.19 (t, J = 9.48Hz, 1 H), 2.97 (m, 1 H), 1.28 (d, J = 6.43 Hz, 6 H), 1.31 (d, J = 6.26Hz, 3 H) 11 4-t-Bu 1,3 pyrazole 1,4 A 507.0 8.17 (s, 1 H), 7.94 (d, J =8.21 Hz, 2 H), 7.91 (d, J = 3.29 Hz, 1 H), 7.68 (d, J = 8.19 Hz, 2 H),phenyl Phenyl [M + H]⁺ 7.65 (d, J = 8.21 Hz, 2 H), 7.46 (d, J = 8.19 Hz,2 H), 6.77 (d, J = 3.29 Hz, 1 H), 5.63 (d, J = 1.85 Hz, 1 H), 3.75 (dd,J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3 H),3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1 H), 3.20 (t, J = 9.48 Hz,1 H), 1.34 (s, 9 H), 1.29 (d, J = 6.26 Hz, 3 H) 12 4-OCF₃ 1,3 pyrazole1,4 A 535.0 8.17 (s, 1 H), 7.95 (d, J = 3.34 Hz, 1 H), 7.91 (d, J = 8.25Hz, 2 H), 7.78 (d, J = 8.28 Hz, 2 H), phenyl Phenyl [M + H]⁺ 7.69 (d, J= 8.25 Hz, 2 H), 7.34 (d, J = 8.28 Hz, 2 H), 6.81 (d, J = 3.34 Hz, 1 H),5.63 (d, J = 1.85 Hz, 1 H), 3.74 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m,1 H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31,3.36 Hz, 1 H), 3.18 (t, J = 9.48 Hz, 1 H), 1.31 (d, J = 6.26 Hz, 3 H) 134-OCF₃ 1,3 5-CO₂Et- 1,4 A 609.0 8.19 (s, 1 H), 7.72 (d, J = 8.34 Hz, 2H), 7.66 (d, J = 8.34 Hz, 2 H), 7.16 (d, J = 8.68 Hz, 2 H), phenylpyrazoline [M + H]⁺ 7.08 (d, J = 8.68 Hz, 2 H), 5.63 (d, J = 1.85 Hz, 1H), 4.87 (dd, J = 2.54, 2.12 Hz, 1 H), 4.25 (q, J = 7.12 Hz, 2 H), 3.68(dd, J = 3.28, 1.99 Hz, 1 H), 3.65 (m, 3 H), 3.59 (s, 3 H), 3.57 (s, 3H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1 H), 3.20 (t, J = 9.48Hz, 1 H), 1.32 (d, J = 6.26 Hz, 3 H), 1.27 (t, J = 7.64 Hz, 3 H) 144-OCF₃ 1,3 5-CO₂-i- 1,4 A 637.0 8.17 (s, 1 H), 7.70 (d, J = 8.36 Hz, 2H), 7.64 (d, J = 8.36 Hz, 2 H), 7.12 (m, 4 H), 5.63 (d, J = phenyl Bu-Phenyl [M + H]⁺ 1.85 Hz, 1 H), 4.89 (dd, J = 2.42, 2.02 Hz, 1 H),3.99-3.91 (m, 4 H), 3.68 (dd, J = 3.28, 1.99 pyrazoline Hz, 1 H), 3.63(m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J =9.31, 3.36 Hz, 1 H), 3.20 (t, J = 9.48 Hz, 1 H), 1.86 (m, 1 H), 1.31 (d,J = 6.26 Hz, 3 H), 0.82 (d, J = 7.12 Hz, 6 H) 15 4-OCF₃ 1,3 pyrazoline1,4 A 537.0 8.17 (s, 1 H), 7.73 (d, J = 8.40 Hz, 2 H), 7.64 (d, J = 8.40Hz, 2 H), 7.12 (d, J = 8.26 Hz, 2 H), phenyl Phenyl [M + H]⁺ 7.09 (d, J= 8.26 Hz, 2 H), 5.63 (d, J = 1.85 Hz, 1 H), 3.89 (t, J = 7.34 Hz, 2 H),3.68 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3 H), 3.57(s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1 H), 3.28 (t, J =7.7 Hz, 2 H), 3.20 (t, J = 9.48 Hz, 1 H), 1.25 (d, J = 6.26 Hz, 3 H) 164-Br 4,1 Imidazole 1,4 A 530.0 8.19 (s, 1 H), 7.97 (s, 1 H), 7.78 (d, J= 8.26 Hz, 2 H), 7.71 (d, J = 8.22 Hz, 2 H), 7.62 (s, 1 H), phenylPhenyl [M]⁺ 7.66 (d, J = 8.26 Hz, 2 H), 7.49 (d, J = 8.22 Hz, 2 H), 5.63(d, J = 1.85 Hz, 1 H), 3.68 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H),3.59 (s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.36Hz, 1 H), 3.20 (t, J = 9.48 Hz, 1 H), 1.25 (d, J = 6.26 Hz, 3 H) 172-CN-3-Cl 1,4 imidazole 1,4 A 510 8.13 (s, 1 H), 7.91 (s, 1 H), 7.81 (d,J = 8.38 Hz, 2 H), 7.71 (d, J = 8.42 Hz, 1 H), 7.70 (d, J = phenylPhenyl [M]⁺ 8.38 Hz, 2 H), 7.68 (s, 1 H), 7.60 (t, 9.51, 1 H), 7.42 (d,J = 8.42 Hz, 1 H), 5.61 (d, J = 1.85 Hz, 1 H), 3.78 (dd, J = 3.28, 1.99Hz, 1 H), 3.69 (m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3 H),3.49 (dd, J = 9.31, 3.36 Hz, 1 H), 3.20 (t, J = 9.48 Hz, 1 H), 1.25 (d,J = 6.26 Hz, 3 H) 18 4-OCF₃ 1,4 imidazole 5- A 566.0 8.70 (s, 1 H), 7.95(d, J = 8.9 Hz, 2 H), 7.51 (d, J = 9.2 Hz, 2 H), 7.39 (d, J = 9.0 Hz, 2H), 7.32 phenyl OCH₃- [M + H]⁺ (d, J = 1.2 Hz, 1 H), 7.16 (d, J = 2.3Hz, 1 H), 6.91 (d, J = 9.2 Hz, 1 H), 5.66 (d, J = 3.3 Hz, 1,2 1 H), 3.88(s, 3 H), 3.76 (dd, J = 3.2, 1.9 Hz, 1 H), 3.71-3.66 (m, 1 H), 3.57 (s,3 H), 3.55 (s, Phenyl 3 H), 3.51 (s, 3 H), 3.50-3.49 (m, 1 H), 3.18 (t,J = 9.5 Hz, 1 H), 1.29 (d, J = 6.6 Hz, 3 H) 19 4-OCF₃ 1,4 imidazole 1,2A 536.0 8.82 (s, 1 H), 8.01 (d, J = 8.0 Hz, 1 H), 7.93 (d, J = 1.5 Hz, 1H), 7.63 (d, J = 7.9 Hz, 1 H), 7.51 phenyl Phenyl [M + H]⁺ (d, J = 9.2Hz, 2 H), 7.44 (t, J = 7.7 Hz, 1 H), 7.39 (d, J = 8.9 Hz, 2 H), 7.34 (d,J = 1.3 Hz, 2 H), 5.68 (d, J = 2.5 Hz, 1 H), 3.77 (dd, J = 3.2, 1.8 Hz,1 H), 3.72-3.67 (m, 1 H), 3.57 (s, 3 H), 3.54 (s, 3 H), 3.51 (s, 3 H),3.49 (d, J = 3.5 Hz, 1 H), 3.19 (t, J = 9.5 Hz, 1 H), 1.29 (d, J = 6.2Hz, 3 H) 20 4-OCF₃ 1,4 imidazole 4- A 566.0 8.78 (s, 1 H), 7.92 (s, 1H), 7.91 (d, J = 1.3 Hz, 1 H), 7.54-7.48 (m, 3 H), 7.38 (d, J = 8.8 Hz,phenyl OCH₃- [M + H]⁺ 2 H), 7.25 (d, J = 1.1 Hz, 1 H), 7.01 (dd, J =8.6, 2.7 Hz, 1 H), 5.69 (d, J = 1.8 Hz, 1 H), 3.89 (s, 1,2 3 H), 3.76(dd, J = 3.6, 1.6 Hz, 1 H), 3.70-3.67 (m, 1 H), 3.57 (s, 3 H), 3.55 (s,3 H), 3.51 (s, Phenyl 3 H), 3.49 (d, J = 3.3 Hz, 1 H), 3.19 (t, J = 9.2Hz, 1 H), 1.29 (d, J = 6.1 Hz, 3 H) 21 4-OCF₃ 1,4 imidazole 2,4- A 572.08.41 (s, 1 H), 8.29-8.22 (m, 1 H), 7.89 (d, J = 1.1 Hz, 1 H), 7.75 (dd,J = 3.8, 1.2 Hz, 1 H), 7.49 phenyl difluoro- [M]⁺ (d, J = 8.9 Hz, 2 H),7.38 (d, J = 8.6 Hz, 2 H), 7.05 (t, J = 9.2 Hz, 1 H), 5.62 (dd, J =57.8, 1.7 1,3 Hz, 1 H), 3.80 (dd, J = 3.4, 2.0 Hz, 1 H), 3.71-3.69 (m, 1H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.55 (d, Phenyl J = 1.8 Hz, 3 H), 3.51(d, J = 1.0 Hz, 1 H), 3.19 (dd, J = 9.1, 4.0 Hz, 1 H), 1.32 (t, J = 6.1Hz, 3 H) 22 6-fluoro- 1,4 imidazole 1,4 A 470 8.37 (s, 1 H), 8.09 (s, 1H), 7.92 (s, 1 H), 7.90 (t, J = 9.32 Hz, 1 H), 7.83 (d, J = 8.30 Hz, 2H), pyrid-2-yl Phenyl [M]⁺ 7.62 (d, J = 8.30 Hz, 2 H), 7.26 (m, 1 H),6.86 (m, 1 H), 5.63 (d, J = 1.85 Hz, 1 H), 3.73 (dd, J = 3.28, 1.99 Hz,1 H), 3.64 (m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44(dd, J = 9.31, 3.36 Hz, 1 H), 3.17 (t, J = 9.48 Hz, 1 H), 1.28 (d, J =6.26 Hz, 3 H) 23 4-iodo- 1,4 imidazole 1,4 A 578 8.37 (s, 1 H), 8.13 (s,1 H), 8.11 (d, J = 8.29 Hz, 1 H), 7.91 (s, 1 H), 7.82 (d, J = 8.26 Hz, 2H), pyrid-2-yl Phenyl [M]⁺ 7.74 (s, 1 H), 7.63 (d, J = 8.26 Hz, 2 H),7.59 (d, J = 8.29 Hz, 1 H), 5.63 (d, J = 1.85 Hz, 1 H), 3.72 (dd, J =3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.56(s, 3 H), 3.42 (dd, J = 9.31, 3.36 Hz, 1 H), 3.18 (t, J = 9.48 Hz, 1 H),1.27 (d, J = 6.26 Hz, 3 H) 24 3,5- 1,4 imidazole 1,4 A 487 8.11 (s, 1H), 7.89 (s, 1 H), 7.79 (d, J = 8.26 Hz, 2 H), 7.65 (d, J = 8.26 Hz, 2H), 7.58 (s, 1 H), difluoro Phenyl [M]⁺ 6.99 (m, 2 H), 6.84 (m, 1 H),5.63 (d, J = 1.85 Hz, 1 H), 3.76 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63phenyl (m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd,J = 9.31, 3.36 Hz, 1 H), 3.18 (t, J = 9.48 Hz, 1 H), 1.28 (d, J = 6.26Hz, 3 H) 25 4-OCF₃ 1,4 imidazole 4- A 566.0 8.59 (s, 1 H), 8.22 (d, J =1.8 Hz, 1 H), 7.96 (dd, J = 8.6, 2.7 Hz, 1 H), 7.88 (d, J = 1.3 Hz, 1H), phenyl OCH₃- [M]⁺ 7.58 (d, J = 1.3 Hz, 1 H), 7.49 (d, J = 8.8 Hz, 2H), 7.37 (d, J = 8.5 Hz, 2 H), 6.80 (d, J = 7.7 1,3 Hz, 1 H), 5.69 (d, J= 1.8 Hz, 1 H), 3.91 (s, 3 H), 3.77 (dd, J = 3.6, 1.6 Hz, 1 H),3.72-3.67 (m, Phenyl 1 H), 3.57 (s, 3 H), 3.55 (s, 3 H), 3.51 (s, 3 H),3.48 (d, J = 3.3 Hz, 1 H), 3.19 (t, J = 9.2 Hz, 1 H), 1.32 (d, J = 6.1Hz, 3 H) 27 4-n-Pr 1,4 imidazole 1,4 A 188 8.18 (s, 1 H), 7.90 (s, 1 H),7.87 (d, J = 7.8 Hz, 2 H), 7.69 (d, J = 7.8 Hz, 2 H), 7.63 (s, 1 H),phenyl Phenyl 7.37 (d, J = 8.4 Hz, 2 H), 7.32 (d, J = 8.4 Hz, 2 H), 5.69(d, J = 1.8 Hz, 1 H), 3.79 (m, 1 H), 3.7 (m, 1 H), 3.63-3.5 (m, 10 H),3.22 (t, J = 6.3 Hz, 1 H), 2.68 (t, J = 8.1 Hz, 2 H), 1.6 (m, 2 H), 1.34(d, J = 6 Hz, 3 H), 1.0 (t, J = 7.5 Hz, 3 H) 28 4-OCF₃ 1,4 imidazole 1,4B 563.0 181 8.20 (s, 1 H), 7.90 (s, 1 H), 7.85 (d, J = 8.5 Hz, 2 H),7.70 (d, J = 8.5 Hz, 2 H), 7.61 (s, 1 H), phenyl Phenyl [M]⁺ 7.42 (d, J= 8.4 Hz, 2 H), 7.40 (d, J = 8.4 Hz, 2 H), 5.62 (d, J = 1.8 Hz, 1 H),3.80-3.5 (m, 9 H), 3.20 (t, J = 9.5 Hz, 1 H), 1.25 (m, 6 H) 29 4-n-Pr1,4 imidazole 1,4 B 194- 8.17 (s, 1 H), 7.90 (s, 1 H), 7.88 (d, J =8.4Hz, 2 H), 7.68 (d, J = 8.4 Hz, 2 H), 7.62 (s, 1 H), phenyl Phenyl 1957.38 (d, J = 8.4 Hz, 2 H), 7.29 (d, J = 8.4 Hz, 2 H), 5.66 (d, J = 1.5Hz, 1 H), 3.74-3.5 (m, 11 H), 3.22 (t, J = 8 Hz, 1 H), 2.68 (t, J = 7.4Hz, 2 H), 1.69 (m, 2 H), 1.33 (m, 6 H), 0.99 (t, J = 7.5 Hz, 3 H) 304-OCF₃ 1,4 imidazole 1,4 A 535.0 8.17 (s, 1 H), 7.93 (s, 1 H), 7.82 (d,J = 8.25 Hz, 2 H), 7.77 (d, J = 8.27 Hz, 2 H), 7.58 (s, 1 H), phenylPhenyl [M + H]⁺ 7.45 (d, J = 8.25 Hz, 2 H), 7.23 (d, J = 8.27 Hz, 2 H),5.63 (d, J = 1.8 Hz, 1 H), 3.7 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31,3.36 Hz, 1 H), 3.20 (t, J = 9.48 Hz, 1 H), 1.25 (d, J = 6.3 Hz, 3 H) 314-OCF₃ 1,4 imidazole 1,4 G 577.6 8.12 (s, 1 H), 7.86 (s, 1 H), 7.81 (d,J = 8.23 Hz, 2 H), 7.66 (d, J = 8.29 Hz, 2 H), 7.63 (s, 1 H), phenylPhenyl [M]⁺ 7.58 (d, J = 8.29 Hz, 2 H), 7.33 (d, J = 8.23 Hz, 2 H), 5.59(d, J = 1.92 Hz, 1 H), 3.91 (dd, J = 9.16, 7.24 Hz, 1 H), 3.83 (dd, J =3.40, 1.92 Hz, 1 H), 3.71-3.57 (m, 7 H), 3.29 (t, J = 9.44 Hz, 1 H),1.33 (d, J = 6.42 Hz, 3 H), 1.26 (td, J = 7.06, 3.66 Hz, 6 H), 1.18 (t,J = 7.20 Hz, 3 H) 32 5-CF₃- 1,4 imidazole 1,4 A 521.0 235 8.79 (s, 1 H),8.47 (s, 1 H), 8.20-8.00 (m, 3 H), 7.90 (d, J = 8.4 Hz, 2 H), 7.69 (d, J= 8.7 Hz, pyrid-2-yl Phenyl [M + H]⁺ 2 H), 7.53 (d, J = 8.6 Hz, 1 H),5.67 (d, J = 1.9 Hz, 1 H), 3.77 (dd, J = 3.3, 2.0 Hz, 1 H), 3.69 (dd, J= 9.7, 6.3 Hz, 1 H), 3.58 (s, 3 H), 3.56 (s, 3 H), 3.54 (s, 3 H), 3.52(m, 1 H), 3.20 (t, J = 9.5 Hz, 1 H), 1.32 (d, J = 6.5 Hz, 3 H) 33 5-CF₃-1,4 imidazole 1,4 G 563.0 194 8.78 (d, J = 2.2 Hz, 1 H), 8.47 (d, J =1.4 Hz, 1 H), 8.17-8.01 (m, 3 H), 7.89 (d, J = 8.5 Hz, pyrid-2-yl Phenyl[M + H]⁺ 2 H), 7.68 (d, J = 8.5 Hz, 2 H), 7.53 (d, J = 8.7 Hz, 2 H),5.58 (d, J = 1.9 Hz, 1 H), 3.93 (dd, J = 9.2, 7.2 Hz, 1 H), 3.82 (dd, J= 3.4, 1.9 Hz, 1 H), 3.78-3.55 (m, 6 H), 3.32 (t, J = 9.5 Hz, 1 H), 1.31(d, J = 6.4 Hz, 3 H), 1.27 (td, J = 7.0, 3.6 Hz, 6 H), 1.20 (t, J = 7.1Hz, 3 H) 34 2-Cl, 5-Br 1,4 imidazole 1,4 A 564 8.15 (s, 1 H), 7.93 (s, 1H), 7.79 (m, 2 H), 7.68 (s, 1 H), 7.56 (s, 1 H), 7.52 (d, J = 8.26 Hz, 2H), phenyl Phenyl [M]⁺ 7.43 (d, J = 8.26 Hz, 2 H), 5.61 (d, J = 1.85 Hz,1 H), 3.78 (dd, J = 3.28, 1.99 Hz, 1 H), 3.69 (m, 1 H), 3.59 (s, 3 H),3.57 (s, 3 H), 3.56 (s, 3 H), 3.49 (dd, J = 9.31, 3.36 Hz, 1 H), 3.20(t, J = 9.48 Hz, 1 H), 1.25 (d, J = 6.26 Hz, 3 H) 35 4-OCF₃ 1,4imidazole 6- A 566.0 8.42 (d, J = 1.7 Hz, 1 H), 8.18 (s, 1 H), 7.89 (d,J = 1.5 Hz, 1 H), 7.86 (s, 1 H), 7.66 (dd, J = 8.7, phenyl OCH₃- [M]⁺2.1 Hz, 1 H), 7.50 (d, J = 8.9 Hz, 2 H), 7.36 (d, J = 9.0 Hz, 2 H), 6.99(d, J = 8.6 Hz, 2 H), 5.66 1,3 (d, J = 2.1 Hz, 1 H), 4.01 (s, 3 H), 3.77(dd, J = 3.2, 2.1 Hz, 1 H), 3.72-3.67 (m, 1 H), 3.58 (s, Phenyl 3 H),3.56-3.53 (m, 6 H), 3.52-3.50 (m, 1 H), 3.20 (t, J = 9.5 Hz, 1 H), 1.32(d, J = 5.8 Hz, 3 H) 36 4-OCF₃ 1,4 imidazole 3- A 553.0 8.41 (s, 1 H),7.92 (t, J = 7.7 Hz, 1 H), 7.88 (d, J = 1.3 Hz, 1 H), 7.61 (d, J = 1.1Hz, 2 H), 7.57 phenyl fluoro- [M]⁺ (s, 1 H), 7.49 (d, J = 9.1 Hz, 2 H),7.38 (d, J = 8.6 Hz, 2 H), 5.67 (d, J = 2.9 Hz, 1 H), 3.77 (dd, 1,4 J =3.3, 2.0 Hz, 1 H), 3.72-3.67 (m, 1 H), 3.58 (s, 3 H), 3.56 (s, 3 H),3.54 (s, 3 H), 3.51 (d, J = Phenyl 3.8 Hz, 1 H), 3.20 (t, J = 9.5 Hz, 1H), 1.32 (d, J = 6.5 Hz, 3 H) 37 4- 1,4 imidazole 1,4 A 549 8.17 (s, 1H), 7.83 (s, 1 H), 7.82 (d, J = 8.22 Hz, 2 H), 7.64 (d, J = 8.22 Hz, 2H), 7.57 (s, 1 H), OCH₂CF₃ Phenyl [M]⁺ 7.39 (d, J = 8.23 Hz, 2 H), 7.07(d, J = 8.23 Hz, 2 H), 5.63 (d, J = 1.85 Hz, 1 H), 4.41 (q, J = phenyl8.24 Hz, 2 H), 3.74 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59(s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1H), 3.20 (t, J = 9.48 Hz, 1 H), 1.29 (d, J = 6.26 Hz, 3 H) 38 3,4,5,6-1,4 imidazole 1,4 A 524 8.08 (s, 1 H), 7.98 (s, 1 H), 7.78 (d, J = 8.29Hz, 2 H), 7.61 (s, 1 H), 7.59 (d, J = 8.29 Hz, 2 H), tetrafluoro- Phenyl[M]⁺ 5.58 (d, J = 1.85 Hz, 1 H), 3.68 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63(m, 1 H), 3.59 (s, 3 H), 3.57 pyrid-2-yl (s, 3 H), 3.56 (s, 3 H), 3.44(dd, J = 9.31, 3.36 Hz, 1 H), 3.16 (t, J = 9.48 Hz, 1 H), 1.22 (d, J =6.26 Hz, 3 H) 39 5-iodo- 1,4 imidazole 1,4 A 578 8.67 (s, 1 H), 8.33 (s,1 H), 8.14 (s, 1 H), 8.08 (d, J = 8.32 Hz, 1 H), 7.91 (s, 1 H), 7.83 (d,J = pyrid-2-yl Phenyl [M]⁺ 8.24 Hz, 2 H), 7.62 (d, J = 8.24 Hz, 2 H),7.21 (d, J = 8.32 Hz, 1 H), 5.63 (d, J = 1.85 Hz, 1 H), 3.74 (dd, J =3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.56(s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1 H), 3.16 (t, J = 9.48 Hz, 1 H),1.29 (d, J = 6.26 Hz, 3 H) 40 4-CF₃ 1,4 imidazole 6- A 550.0 176- 8.43(s, 1 H), 8.18 (s, 1 H), 7.95 (d, J = 15.4 Hz, #H), 7.78 (d, J = 7.4 Hz,2 H), 7.64-7.58 (m, phenyl OCH₃- [M + H]⁺ 178 2 H), 7.25 (d, J = 3.8 Hz,1 H), 6.99 (d, J = 7.7 Hz, 1 H), 5.66 (s, 1 H), 4.02 (s, 3 H), 3.78-3.751,3 (m, 2 H), 3.58-3.53 (m, 10 H), 3.22-3.20 (m, 1 H), 1.31 (d, J = 5.8Hz, 3 H) Phenyl 41 4-CH₃ 1,4 imidazole 1,4 A 465 8.12 (s, 1 H), 7.84 (s,1 H), 7.82 (d, J = 8.31 Hz, 2 H), 7.63 (d, J = 8.31 Hz, 2 H), 7.56 (s, 1H), phenyl Phenyl [M]⁺ 7.28 (s, 4 H), 5.63 (d, J = 1.85 Hz, 1 H), 3.73(dd, J = 3.28, 1.99 Hz, 1 H), 3.65 (m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3H), 3.56 (s, 3 H), 3.32 (dd, J = 9.31, 3.36 Hz, 1 H), 3.17 (t, J = 9.48Hz, 1 H), 2.39 (s, 3 H), 1.29 (d, J = 6.26 Hz, 3 H) 42 4-CF₃ 1,4imidazole 1,4 A 519 8.14 (s, 1 H), 7.96 (s, 1 H), 7.81 (d, J = 8.27 Hz,2 H), 7.74 (d, J = 8.22 Hz, 2 H), 7.65 (d, J = phenyl Phenyl [M]⁺ 8.27Hz, 2 H), 7.63 (s, 1 H), 7.55 (d, J = 8.22 Hz, 2 H), 5.63 (d, J = 1.85Hz, 1 H), 3.75 (dd, J = 3.28, 1.99 Hz, 1 H), 3.67 (m, 1 H), 3.59 (s, 3H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.31 (dd, J = 9.31, 3.36 Hz, 1 H),3.18 (t, J = 9.48 Hz, 1 H), 1.31 (d, J = 6.26 Hz, 3 H) 43 4-Cl 1,4imidazole 1,4 A 485 8.09 (s, 1 H), 7.86 (s, 1 H), 7.81 (d, J = 8.22 Hz,2 H), 7.64 (d, J = 8.22 Hz, 2 H), 7.57 (s, 1 H), phenyl Phenyl [M]⁺ 7.45(d, J = 8.29 Hz, 2 H), 7.37 (d, J = 8.29 Hz, 2 H), 5.63 (d, J = 1.85 Hz,1 H), 3.74 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3 H),3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1 H), 3.17(t, J = 9.48 Hz, 1 H), 1.28 (d, J = 6.26 Hz, 3 H) 44 4-OCH₃ 1,4imidazole 1,4 A 481 8.09 (s, 1 H), 7.83 (d, J = 8.23 Hz, 2 H), 7.76 (s,1 H), 7.61 (d, J = 8.23 Hz, 2 H), 7.51 (s, 1 H), phenyl Phenyl [M]⁺ 7.29(d, J = 8.20 Hz, 2 H), 6.97 (d, J = 8.20 Hz, 2 H), 5.63 (d, J = 1.85 Hz,1 H), 3.82 (s, 3 H), 3.73 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H),3.59 (s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.42 (dd, J = 9.31, 3.36Hz, 1 H), 3.16 (t, J = 9.48 Hz, 1 H), 1.29 (d, J = 6.26 Hz, 3 H) 45 4-Br1,4 imidazole 1,4 A 530 8.12 (s, 1 H), 7.86 (s, 1 H), 7.81 (d, J = 8.23Hz, 2 H), 7.66 (d, J = 8.29 Hz, 2 H), 7.63 (s, 1 H), phenyl Phenyl [M]⁺7.58 (d, J = 8.29 Hz, 2 H), 7.33 (d, J = 8.23 Hz, 2 H), 5.63 (d, J =1.85 Hz, 1 H), 3.74 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59(s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.33 (dd, J = 9.31, 3.36 Hz, 1H), 3.18 (t, J = 9.48 Hz, 1 H), 1.29 (d, J = 6.26 Hz, 3 H) 46 4-i-Pr 1,4imidazole 1,4 A 493 8.37 (s, 1 H), 8.31 (s, 1 H), 8.28 (s, 1 H), 7.79(d, J = 8.23 Hz, 2 H), 7.62 (d, J = 8.23 Hz, 2 H), phenyl Phenyl [M]⁺7.57 (d, J = 8.25 Hz, 2 H), 7.38 (d, J = 8.25 Hz, 2 H), 5.63 (d, J =1.85 Hz, 1 H), 3.75 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59(s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1H), 3.05 (t, J = 9.48 Hz, 1 H), 2.92 (m, 1 H) 1.27 (d, J = 6.46 Hz, 6H), 1.21 (d, J = 6.26 Hz, 3 H) 47 4-I 1,4 imidazole 1,4 A 577 8.16 (s, 1H), 7.87 (s, 1 H), 7.83 (d, J = 8.29 Hz, 2 H), 7.68 (d, J = 8.29 Hz, 2H), 7.57 (s, 1 H), phenyl Phenyl [M]⁺ 7.18 (d, J = 8.24 Hz, 2 H), 6.87(d, J = 8.24 Hz, 2 H), 5.63 (d, J = 1.85 Hz, 1 H), 3.78 (dd, J = 3.28,1.99 Hz, 1 H), 3.69 (m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3H), 3.48 (dd, J = 9.31, 3.36 Hz, 1 H), 3.20 (t, J = 9.48 Hz, 1 H), 1.31(d, J = 6.26 Hz, 3 H) 48 4-t-Bu 1,4 imidazole 1,4 A 507 8.13 (s, 1 H),7.86 (s, 1 H), 7.82 (d, J = 8.28 Hz, 2 H), 7.62 (d, J = 8.28 Hz, 2 H),7.58 (s, 1 H), phenyl Phenyl [M]⁺ 7.48 (d, J = 8.26 Hz, 2 H), 7.36 (d, J= 8.26 Hz, 2 H), 5.63 (d, J = 1.85 Hz, 1 H), 3.73 (dd, J = 3.28, 1.99Hz, 1 H), 3.65 (m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3 H),3.45 (dd, J = 9.31, 3.36 Hz, 1 H), 3.18 (t, J = 9.48 Hz, 1 H), 1.37 (s,9 H), 1.25 (d, J = 6.26 Hz, 3 H) 49 4-OCF₃ 1,4 imidazole 2,3- A 554.08.40 (s, 1 H), 7.99 (t, J = 8.0 Hz, 1 H), 7.93 (s, 1 H), 7.79 (dd, J =3.2, 1.1 Hz, 1 H), 7.72 (t, J = phenyl difluoro- [M]⁺ 7.5 Hz, 1 H), 7.51(d, J = 8.9 Hz, 2 H), 7.39 (d, J = 8.4 Hz, 2 H), 5.67 (s, 1 H), 3.77(dd, J = 3.2, 1,4 1.9 Hz, 1 H), 3.71-3.67 (m, 1 H), 3.58-3.55 (m, 6 H),3.51 (s, 3 H), 3.42 (dd, J = 9.5, 3.5 Hz, Phenyl 1 H), 3.21 (t, J = 9.8Hz, 1 H), 1.32 (d, J = 5.7 Hz, 3 H) 50 4-OCF₃ 1,4 imidazole 6-Cl-1,3 A570.0 8.38 (d, J = 3.1 Hz, 1 H), 8.19 (s, 1 H), 8.03 (d, J = 1.0 Hz, 1H), 7.91 (d, J = 1.1 Hz, 1 H), 7.60 phenyl Phenyl [M + H]⁺ (dd, J = 8.2,2.2 Hz, 1 H), 7.51 (d, J = 8.7 Hz, 2 H), 7.45 (d, J = 8.4 Hz, 1 H), 7.38(d, J = 9.5 Hz, 2 H), 5.66 (d, J = 3.0 Hz, 1 H), 3.76 (dd, J = 3.2, 1.9Hz, 1 H), 3.70-3.65 (m, 1 H), 3.58 (s, 3 H), 3.55 (s, 3 H), 3.54 (s, 3H), 3.50 (dd, J = 6.4, 3.3 Hz, 1 H), 3.20 (t, J = 9.5 Hz, 1 H), 1.31 (d,J = 5.5 Hz, 3 H) 51 4- 1,4 imidazole 1,4 A 585 8.17 (s, 1 H), 8.91 (s, 1H), 7.84 (d, J = 8.22 Hz, 2 H), 7.68 (d, J = 8.22 Hz, 2 H), 7.61 (s, 1H), OCF₂CF₃ Phenyl [M]⁺ 7.47 (d, J = 8.27 Hz, 2 H), 7.39 (d, J = 8.27Hz, 2 H), 5.63 (d, J = 1.85 Hz, 1 H), 3.79 (dd, J = phenyl 3.28, 1.99Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3 H),3.44 (dd, J = 9.31, 3.36 Hz, 1 H), 3.20 (t, J = 9.48 Hz, 1 H), 1.30 (d,J = 6.26 Hz, 3 H) 52 4- 1,4 imidazole 1,4 G 627 8.12 (s, 1 H), 7.91 (s,1 H), 7.84 (d, J = 8.26 Hz, 2 H), 7.63 (d, J = 8.26 Hz, 2 H), 7.61 (s, 1H), OCF₂CF₃ Phenyl [M]⁺ 7.49 (d, J = 8.34 Hz, 2 H), 7.37 (d, J = 8.34Hz, 2 H), 5.59 (d, J = 1.9 Hz, 1 H), 3.91 (dd, J = phenyl 9.16, 7.24 Hz,1 H), 3.83 (dd, J = 3.40, 1.92 Hz, 1 H), 3.71-3.57 (m, 7 H), 3.29 (t, J= 9.44 Hz, 1 H), 1.33 (d, J = 6.42 Hz, 3 H), 1.26 (td, J = 7.06, 3.66Hz, 6 H), 1.18 (t, J = 7.20 Hz, 3 H) 53 4-OCF₃ 1,3 4-5- 1,4 A 681.0 8.18(s, 1 H), 7.85 (d, J = 8.26 Hz, 2 H), 7.66 (d, J = 8.26 Hz, 2 H), 7.18(s, 4 H), 5.63 (d, J = phenyl di(CO₂Et) Phenyl [M + H]⁺ 1.85 Hz, 1 H),5.20 (d, 5.34 Hz, 1 H), 4.58 (d, J = 5.34 Hz, 1 H), 4.21 (m, 4 H), 3.68(dd, J = pyrazoline 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3 H),3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1 H), 3.20(t, J = 9.48 Hz, 1 H), 1.25 (d, J = 6.26 Hz, 3 H), 1.23 (m, 6 H) 544-OCF₃ 1,3 5-CO₂Me- 1,4 A 595.0 8.17 (s, 1 H), 7.71 (d, J = 8.38 Hz, 2H), 7.65 (d, J = 8.38 Hz, 2 H), 7.17 (d, J = 8.30 Hz, 2 H), phenylpyrazoline Phenyl [M + H]⁺ 7.08 (d, J = 8.30 Hz, 2 H), 5.63 (d, J = 1.85Hz, 1 H), 4.83 (dd, J = 2.42, 1.98 Hz, 1 H), 3.79 (s, 3 H), 3.77-3.62(m, 4 H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J =9.31, 3.36 Hz, 1 H), 3.20 (t, J = 9.48 Hz, 1 H), 1.25 (d, J = 6.26 Hz, 3H) 55 4-OCF₃ 1,3 4-n-Pr-5- 1,4 A 651.0 8.16 (s, 1 H), 7.74 (d, J = 8.22Hz, 2 H), 7.62 (d, J = 8.22 Hz, 2 H), 7.14 (d, J = 8.18 Hz, 2 H), phenylCO₂Et- Phenyl [M]⁺ 7.07 (d, J = 8.18 Hz, 2 H), 5.63 (d, J = 1.85 Hz, 1H), 4.59 (d, J = 5.36 Hz, 1 H), 4.19 (q, J = pyrazoline 7.20 Hz, 2 H),3.78 (dd, J = 3.28, 1.99 Hz, 1 H), 3.72-3.49 (m, 15 H), 3.44 (dd, J =9.31, 3.36 Hz, 1 H), 3.20 (t, J = 9.48 Hz, 1 H), 1.36-1.24 (m, 6 H),1.21 (t, J = 9.40 Hz, 3 H) 56 4-OCF₃ 1,3 4-CH₃-5- 1,4 A 623.0 8.16 (s, 1H), 7.72 (d, J = 8.22 Hz, 2 H), 7.63 (d, J = 8.22 Hz, 2 H), 7.12 (d, J =8.34 Hz, 2 H), phenyl CO₂Et- Phenyl [M]⁺ 7.08 (d, J = 8.34 Hz, 2 H),5.63 (d, J = 1.85 Hz, 1 H), 4.42 (d, J = 5.22 Hz, 1 H), 4.19 (q, J =pyrazoline 7.02 Hz, 2 H), 3.71-3.63 (m, 3 H), 3.59 (s, 3 H), 3.57 (s, 3H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1 H), 3.20 (t, J = 9.48Hz, 1 H), 1.28 (d, J = 6.26 Hz, 3 H), 1.22-1.17 (m, 6 H) 57 4-CF₃ 4,1imidazole 1,4 A 519.0 104 8.21 (s, 1 H), 7.98 (s, 1 H), 7.91 (d, J = 8.2Hz, 2 H), 7.80 (d, J = 8.0 Hz, 2 H), 7.70 (s, 1 H), Phenyl [M + H]⁺ 7.68(d, J = 8.2 Hz, 2 H), 7.5 (d, J = 8.3 Hz, 2 H), 5.68 (d, J = 1.8 Hz, 1H), 3.78 (m, 1 H), 3.68 (m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.56 (s,3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1 H), 3.20 (t, J = 9.48 Hz, 1 H),1.25 (d, J = 6.3 Hz, 3 H) 58 4-OCF₃ 1,4 imidazole 1,3 A 536.4 8.21 (s, 1H), 8.12 (s, 1 H), 7.91 (s, 1 H), 7.89 (s, 1 H), 7.62 (s, 1 H), 7.53 (d,J = 7.9 Hz, 1 H), phenyl Phenyl [M + H]⁺ 7.50 (d, J = 8.9 Hz, 2 H), 7.45(d, J = 7.3 Hz, 1 H), 7.37 (d, J = 8.6 Hz, 2 H), 5.68 (d, J = 2.6 Hz, 1H), 3.78 (dd, J = 2.8, 2.0 Hz, 1 H), 3.72-3.67 (m, 1 H), 3.58 (s, 3 H),3.56 (s, 3 H), 3.55 (s, 3 H), 3.52-3.49 (m, 1 H), 3.21 (t, J = 9.3 Hz, 1H), 1.32 (d, J = 6.5 Hz, 3 H) 59 3-CF₃, 4- 1,4 imidazole 1,4 A 604.58.18 (s, 1 H), 7.92 (d, J = 2 Hz, 1 H), 7.88 (d, J = 8.4 Hz, 2 H), 7.8(d, J = 3 Hz, 1 H), 7.74-7.68 OCF₃ Phenyl [M + H]⁺ (m, 3 H), 7.64 (d, J= 2 Hz, 1 H), 7.6 (d, J = 8 Hz, 1 H), 5.64 (d, J = 1.9 Hz, 1 H), 3.81(dd, J = phenyl 9.2, 7.2 Hz, 1 H), 3.75 (dd, J = 3.40, 1.9 Hz, 1 H),3.71-3.57 (m, 7 H), 3.21 (t, J = 9.4 Hz, 1 H), 1.33 (d, J = 6.4 Hz, 3 H)60 4-n-Pr 5,3 isoxazole 1,4 A 494.0 8.18 (s, 1 H), 7.89 (d, J = 8.22 Hz,2 H), 7.74 (d, J = 8.44 Hz, 2 H), 7.71 (d, J = 8.22 Hz, 2 H), phenylPhenyl [M]⁺ 7.31 (d, J = 8.44 Hz, 2 H), 6.81 (s, 1 H), 5.63 (d, J = 1.85Hz, 1 H), 3.68 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1 H),3.20 (t, J = 9.48 Hz, 1 H), 2.68 (t, J = 7.24 Hz, 2 H), 1.68 (m, 2 H),1.31 (d, J = 6.26 Hz, 3 H), 0.98 (t, J = 7.12 Hz, 3 H) 61 4-n-BuO- 5,3isoxazole 1,4 A 524.0 8.19 (s, 1 H), 7.89 (d, J = 8.34 Hz, 2 H), 7.74(d, J = 8.46 Hz, 2 H), 7.71 (d, J = 8.34 Hz, 2 H), phenyl Phenyl [M]⁺6.98 (d, J = 8.46 Hz, 2 H), 6.67 (s, 1 H), 5.63 (d, J = 1.85 Hz, 1 H),4.04 (t, J = 7.88 Hz, 2 H), 3.68 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m,1 H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31,3.36 Hz, 1 H), 3.20 (t, J = 9.48 Hz, 1 H), 1.79 (m, 2 H), 1.54 (m, 2 H),1.32 (d, J = 6.26 Hz, 3 H), 0.99 (t, J = 7.26 Hz, 3 H) 62 4-CH₃O- 2,4thiazole 1,4 A 499.0 74-80 8.18 (s, 1 H), 8.02 (d, J = 6.0 Hz, 2 H),7.98 (d, J = 6.0 Hz, 2 H), 7.70 (d, J = 6.0 Hz, 2 H), 7.48 phenyl Phenyl[M + H]⁺ (s, 1 H), 6.98 (d, J = 6.0 Hz, 2 H), 5.68 (d, J = 3.0 Hz, 1 H),3.88 (s, 3 H), 3.77-3.76 (m, 1 H), 3.71-3.67 (m, 1 H), 3.58 (s, 3 H),3.56 (s, 3 H), 3.54 (s, 3 H), 3.54-3.50 (m, 1 H), 3.20 (t, J = 9.0 Hz, 1H), 1.32 (d, J = 6.0 Hz, 3 H) 63 3-Cl-5- 2,4 thiazole 1,4 A 574.0 8.78(s, 1 H), 8.19 (s, 1 H), 8.13 (d, J = 3.0 Hz, 1 H), 8.05 (d, J = 9.0 Hz,2 H), 7.81 (s, 1 H), CF₃-pyrid- Phenyl [M + H]⁺ 7.73 (d, J = 6.0 Hz, 2H), 5.69 (d, J = 3.0 Hz, 1 H), 3.78-3.77 (m, 1 H), 3.72-3.68 (m, 1 H),3.59 2-yl (s, 3 H), 3.56 (s, 3 H), 3.55 (s, 3 H), 3.53 (dd, J = 6.0, 3.0Hz, 1 H), 3.21 (t, J = 9.0 Hz, 1 H), 1.33 (d, J = 6.0 Hz, 3 H) 64 6- 2,4thiazole 1,4 A 569.0 142-145 8.78 (d, J = 3 Hz, 1 H), 8.32 (dd, J = 6.0,3.0 Hz, 1 H), 8.2 (s, 1 H), 8.01 (d, J = 6.0 Hz, 2 H), CF₃CH₂O- Phenyl[M + H]⁺ 7.71 (d, J = 6.0 Hz, 2 H), 7.55 (s, 1 H), 6.98 (d, J = 6.0 Hz,1 H), 5.68 (d, J = 3.0 Hz, 1 H), 4.83 pyrid-3-yl (q, J = 6.0 Hz, 2 H),3.77 (m, 1 H), 3.69 (m, 1 H), 3.58 (s, 3 H), 3.56 (s, 3 H), 3.54 (s, 3H), 3.52 (dd, J = 6.0, 3.0 Hz, 1 H), 3.20 (t, J = 9.0 Hz, 1 H), 1.32 (d,J = 6.0 Hz, 3 H) 65 4-CF₃- 2,4 thiazole 1,4 A 537.0 166-168 8.19 (s, 1H), 8.16 (d, J = 6.0 Hz, 2 H), 8.03 (d, J = 6.0 Hz, 2 H), 7.74-7.71 (m,4 H), 7.63 (s, phenyl Phenyl [M + H]⁺ 1 H), 5.68 (s, 1 H), 3.78-3.76 (m,1 H), 3.71-3.67 (m, 1 H), 3.58 (s, 3 H), 3.56 (s, 3 H), 3.54 (s, 3 H),3.53-3.50 (m, 1 H), 3.21 (t, J = 9.0 Hz, 1 H), 1.33 (d, J = 3.0 Hz, 3 H)66 6-CF₃- 2,4 thiazole 1,4 A 539.0 167- 9.33 (s, 1 H), 8.52 (dd, J =7.5, 3.0 Hz, 1 H), 8.19 (s, 1 H), 8.03 (d, J = 6.0 Hz, 2 H), 7.81 (d, J= pyrid-3-yl Phenyl [M + H]⁺ 169 6.0, 1 H), 7.74 (d, J = 6.0 Hz, 2 H),7.70 (s, 1 H), 5.69 (d, J = 3.0 Hz, 1 H), 3.78-3.77 (m, 1 H), 3.71-3.67(m, 1 H), 3.59 (s, 3 H), 3.56 (s, 3 H), 3.55 (s, 3 H), 3.52 (dd, J =9.0,3.0 Hz, 1 H), 1.33 (d, J = 3.0 Hz, 3 H) 67 4-OCF₃ 1,3 pyrrole 1,4 A 5348.15 (s, 1 H), 7.63 (s, 1 H), 7.60 (d, J = 8.48 Hz, 2 H), 7.49 (d, J =8.48 Hz, 2 H), 7.25-7.19 (m, phenyl Phenyl [M]⁺ 4 H), 6.98 (d, J = 5.88Hz, 1 H), 6.71 (d, J = 5.86 Hz, 1 H), 5.63 (d, J = 1.85 Hz, 1 H), 3.68(dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1 H), 3.20 (t, J = 9.48Hz, 1 H), 1.25 (d, J = 6.26 Hz, 3 H) 68 4-OCF₃ 4,2 4,5-dihydro- 1,4 B552 8.19 (s, 1 H), 8.08 (d, J = 8.26 Hz, 2 H), 7.72 (d, J = 8.26 Hz, 2H), 7.32 (d, J = 8.24 Hz, 2 H), phenyl 1,3-oxazole Phenyl [M + H]⁺ 7.20(d, J = 8.24 Hz, 2 H), 5.63 (d, J = 1.85 Hz, 1 H), 5.42 (t, J = 9.42 Hz,1 H), 8.84 (t, J = 9.46, 1 H), 4.28 (t, J = 9.46 Hz, 1 H), 3.79-3.61 (m,4 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1 H),3.18 (t, J = 9.48 Hz, 1 H), 1.36-1.23 (m, 6 H) 69 5-Cl- 3,1 1,2,4- 1,4 A487.0 8.77-8.69 (m, 2 H), 8.21-8.17 (m, 2 H), 7.89-7.73 (m, 5 H), 5.63(d, J = 1.85 Hz, 1 H), 3.68 (dd, pyrid-2-yl triazole Phenyl [M + H]⁺ J =3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.56(s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1 H), 3.20 (t, J = 9.48 Hz, 1 H),1.25 (d, J = 6.26 Hz, 3 H) 70 2-F 3,1 1,2,4- 1,4 A 470.0 9.41 (s, 1 H),8.24 (s, 1 H), 8.19-8.17 (m, 1 H), 7.91 (d, J = 8.25 Hz, 2 H), 7.79-7.69(m, 1 H), phenyl triazole Phenyl [M]⁺ 7.58 (d, J = 8.25 Hz, 2 H),7.16-7.08 (m, 1 H), 6.89-6.84 (m, 1 H), 5.63 (d, J = 1.85 Hz, 1 H), 3.68(dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1 H), 3.20 (t, J = 9.48Hz, 1 H), 1.25 (d, J = 6.26 Hz, 3 H) 71 pyrid-3-yl 3,1 1,2,4- 1,4 A453.0 9.51 (s, 1 H), 9.28 (s, 1 H), 8.69-8.67 (m, 1 H), 8.48 (s, 1 H),8.42-8.40 (m, 1 H), 8.08 (d, J = triazole Phenyl [M]⁺ 8.30 Hz, 2 H),7.84 (d, J = 8.30 Hz, 2 H), 7.58-7.52 (m, 1 H), 5.63 (d, J = 1.85 Hz, 1H), 3.68 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3 H),3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1 H), 3.20(t, J = 9.48 Hz, 1 H), 1.25 (d, J = 6.26 Hz, 3 H) 72 4-CF₃ 3,1 1,2,4-1,4 A 522.0 166 8.66 (s, 1 H), 8.33 (d, J =7.9 Hz, 2 H), 8.20 (s, 1 H),7.81 (s, 4 H), 7.74 (d, J = 8.4 Hz, 2 H), phenyl triazole Phenyl [M +H]⁺ 5.68 (d, J = 1.9 Hz, 1 H), 3.77 (dd, J = 3.2, 2.0 Hz, 1 H), 3.68(dd, J = 9.6, 6.2 Hz, 1 H), 3.59 (s, 3 H), 3.56 (s, 3 H), 3.55 (s, 3 H),3.51 (m, 1 H), 3.21 (t, J = 9.3 Hz, 1 H), 1.33 (d, J = 6.1 Hz, 3 H) 73phenyl 1,3 pyrazoline 1,4 A 454.2 8.17 (s, 1 H), ), 7.73 (d, J = 8.40Hz, 2 H), 7.64 (d, J = 8.40 Hz, 2 H), 7.33 (m, 2 H), 7.18 (d, J = Phenyl[M + H]⁺ 7 Hz, 2 H), 6.89 (t, J = 7 Hz, 1 H), 5.68 (s, 1 H), 3.95 (t, J= 9 Hz, 2 H), 3.78 (m, 1 H), 3.6 (m, 1 H), 3.6-3.5 (m, 10 H), 3.28 (t, J= 9 Hz, 2 H), 3.21 (t, J = 8 Hz, 1 H), 1.34 (d, J = 6.3 Hz, 3 H) 744-CF₃ 3,1 1,2,4- 1,4 C 549.0 170- 8.66 (s, 1 H), 8.35 (d, J = 7.9 Hz, 2H), 8.20 (s, 1 H), 7.81 (s, 4 H), 7.74 (d, J = 8.4 Hz, 2 H), phenyltriazole Phenyl [M + H]⁺ 175 5.66 (d, J = 1.8 Hz, 1 H), 3.77 (m, 1 H),3.68-3.5 (m, 10 H), 3.21 (t, J = 9.2 Hz, 1 H), 1.7 (m, 2 H), 1.33 (d, J= 6.2 Hz, 3 H), 0.98 (t, J = 7.5 Hz, 3 H) 75 4-Cl 1,4 1,2,3- 1,4 A 486.08.19 (s, 1 H), 8.17 (s, 1 H), 7.93 (d, J = 8.22 Hz, 2 H), 7.72 (d, J =8.20 Hz, 2 H), 7.60 (d, J = phenyl triazole Phenyl [M]⁺ 8.22 Hz, 2 H),7.51 (d, J = 8.20 Hz, 2 H), 5.63 (d, J = 1.85 Hz, 1 H), 3.68 (dd, J =3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.56(s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1 H), 3.20 (t, J = 9.48 Hz, 1 H),1.25 (d, J = 6.26 Hz, 3 H) 76 4-CH₃ 1,4 1,2,3- 1,4 A 466.0 8.19 (s, 1H), 8.18 (s, 1 H), 7.96 (d, J = 8.26 Hz, 2 H), 7.70 (d, J = 8.26 Hz, 2H), 7.67 (d, J = phenyl triazole Phenyl [M]⁺ 8.30 Hz, 2 H), 7.37 (d, J =8.30 Hz, 2 H), 5.63 (d, J = 1.85 Hz, 1 H), 3.68 (dd, J = 3.28, 1.99 Hz,1 H), 3.63 (m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44(dd, J = 9.31, 3.36 Hz, 1 H), 3.20 (t, J = 9.48 Hz, 1 H), 2.42 (s, 3 H),1.25 (d, J = 6.26 Hz, 3 H) 77 4-OCH₃ 1,4 1,2,3- 1,4 A 482.0 8.17 (s, 1H), 8.16 (s, 1 H), 7.92 (d, J = 8.32 Hz, 2 H), 7.69 (d, J = 8.32 Hz, 2H), 7.64 (d, J = phenyl triazole Phenyl [M]⁺ 8.23 Hz, 2 H), 7.04 (d, J =8.23 Hz, 2 H), 5.63 (d, J = 1.85 Hz, 1 H), 3.86 (s, 3 H), 3.71 (dd, J =3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.56(s, 3 H), 3.42 (dd, J = 9.31, 3.36 Hz, 1 H), 3.19 (t, J = 9.48 Hz, 1 H),1.29 (d, J = 6.26 Hz, 3 H) 78 4-CF₃ 1,4 1,2,3- 1,4 A 520.0 8.28 (s, 1H), 8.18 (s, 1 H), 7.97 (d, J = 8.48 Hz, 2 H), 7.92 (d, J = 8.36 Hz, 2H), 7.83 (d, J = phenyl triazole Phenyl [M]⁺ 8.48 Hz, 2 H), 7.76 (d, J =8.36 Hz, 2 H), 5.63 (d, J = 1.85 Hz, 1 H), 3.74 (dd, J = 3.28, 1.99 Hz,1 H), 3.63 (m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44(dd, J = 9.31, 3.36 Hz, 1 H), 3.20 (t, J = 9.48 Hz, 1 H), 1.28 (d, J =6.26 Hz, 3 H) 79 4-OCF₃ 1,4 1,2,3- 1,4 A 536.0 9.39 (s, 1 H), 8.41 (s, 1H), 8.08 (d, J = 8.22 Hz, 2 H), 7.98 (d, J = 8.28 Hz, 2 H), 7.78 (d, J =phenyl triazole Phenyl [M]⁺ 8.22 Hz, 2 H), 7.66 (d, J = 8.28 Hz, 2 H),5.63 (d, J = 1.85 Hz, 1 H), 3.77 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m,1 H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31,3.36 Hz, 1 H), 3.17 (t, J = 9.48 Hz, 1 H), 1.26 (d, J = 6.26 Hz, 3 H) 804-CF₃ 1,3 1,2,4- 1,4 A 521.0 175- 8.69 (s, 1 H), 8.25 (d, J = 8.7 Hz, 2H), 8.20 (s, 1 H), 7.93 (d, J = 8.4 Hz, 2 H), 7.82 (d, J = 8.7 phenyltriazole Phenyl [M + H]⁺ 176 Hz, 2 H), 7.76 (d, J = 8.4 Hz, 2 H), 5.67(d, J = 2.1 Hz, 1 H), 3.8-3.65 (m, 2 H), 3.65 (s, 3 H), 3.58 (s, 3 H),3.56 (s, 3 H), 3.6 (m, 1 H), 3.25 (t, J = 9.3 Hz, 1 H), 1.33 (d, J = 6.3Hz, 3 H) 81 4-n-Bu 1,3 1,2,4- 1,4 A 509.1 142 8.51 (s, 1 H), 8.33 (d, J= 8 Hz, 2 H), 8.20 (s, 1 H), 7.75 (d, J = 8 Hz, 2 H), 7.65 (d, J = 8.2Hz, phenyl triazole Phenyl [M + H]⁺ 2 H), 7.33 (d, J = 8.2 Hz, 2 H),5.68 (d, J = 1.9 Hz, 1 H), 3.77 (dd, J = 3.2, 2.0 Hz, 1 H), 3.68 (dd, J= 9.6, 6.2 Hz, 1 H), 3.59 (s, 3 H), 3.56 (s, 3 H), 3.55 (s, 3 H), 3.51(m, 1 H), 3.21 (t, J = 9.3 Hz, 1 H), 2.70 (t, J = 7.8 Hz, 2 H), 1.65 (m,2 H), 1.38 (m, 2 H), 1.33 (d, J = 6.1 Hz, 3 H), 0.95 (t, J = 7.5 Hz, 3H) 82 4-OCF₃ 1,3 1,2,4- 1,4 A 536 8.59 (s, 1 H), 8.22 (d, J = 8.3 Hz, 2H), 8.18 (s, 1 H), 7.81 (d, J = 8.3 Hz, 2 H), 7.67 (d, J = 8.3 phenyltriazole Phenyl [M]⁺ Hz, 2 H), 7.39 (d, J = 8.3 Hz, 2 H), 5.63 (d, J =1.8 Hz, 1 H), 3.78 (dd, J = 3.3, 2.0 Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.4 Hz, 1 H), 3.20(t, J = 9.48 Hz, 1 H), 1.28 (d, J = 6.26 Hz, 3 H) 83 4-i-Pr 1,3 1,2,4-1,4 A 494.0 8.53 (s, 1 H), 8.21 (d, J = 8.29 Hz, 2 H), 8.17 (s, 1 H),7.72 (d, J = 8.29 Hz, 2 H), 7.63 (d, J = phenyl triazole Phenyl [M]⁺8.25 Hz, 2 H), 7.36 (d, J = 8.25 Hz, 2 H), 5.63 (d, J = 1.85 Hz, 1 H),3.70 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3 H), 3.57(s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1 H), 3.20 (t, J =9.48 Hz, 1 H), 2.97 (m, 1 H), 1.31 (d, J = 6.12 Hz, 3 H), 1.29 (d, J =6.12 Hz, 3 H), 1.25 (d, J = 6.26 Hz, 3 H) 84 4-Cl 1,3 1,2,4- 1,4 A 4878.58 (s, 1 H), 8.21 (d, J = 8.26 Hz, 2 H), 8.18 (s, 1 H), 7.74 (d, J =8.24 Hz, 2 H), 7.72 (d, J = phenyl triazole Phenyl [M + H]⁺ 8.26 Hz, 2H), 7.49 (d, J = 8.24 Hz, 2 H), 5.63 (d, J = 1.85 Hz, 1 H), 3.71 (dd, J= 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.56(s, 3 H), 3.41 (dd, J = 9.31, 3.36 Hz, 1 H), 3.17 (t, J = 9.48 Hz, 1 H),1.29 (d, J = 6.26 Hz, 3 H) 85 4-OCH₃ 1,3 1,2,4- 1,4 A 482 8.41 (s, 1 H),8.22 (s, 1 H), 8.18 (d, J = 8.27 Hz, 2 H), 7.69 (d, J = 8.26 Hz, 2 H),7.59 (d, J = phenyl triazole Phenyl [M]⁺ 8.27 Hz, 2 H), 6.99 (d, J =8.26 Hz, 2 H), 5.63 (d, J = 1.85 Hz, 1 H), 3.82 (s, 3 H), 3.76 (dd, J =3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.56(s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1 H), 3.19 (t, J = 9.48 Hz, 1 H),1.32 (d, J = 6.26 Hz, 3 H) 86 4-t-Bu 1,3 1,2,4- 1,4 A 508 8.52 (s, 1 H),8.21 (d, J = 8.23 Hz, 2 H), 8.17 (s, 1 H), 7.71 (d, J = 8.23 Hz, 2 H),7.62 (d, J = phenyl triazole Phenyl [M]⁺ 8.26 Hz, 2 H), 7.51 (d, J =8.26 Hz, 2 H), 5.63 (d, J = 1.85 Hz, 1 H), 3.72 (dd, J = 3.28, 1.99 Hz,1 H), 3.63 (m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44(dd, J = 9.31, 3.36 Hz, 1 H), 3.19 (t, J = 9.48 Hz, 1 H), 1.34 (s, 9 H),1.28 (d, J = 6.26 Hz, 3 H) 87 4-SCF₃ 1,3 1,2,4- 1,4 A 552.0 8.66 (s, 1H), 8.24 (d, J = 8.28 Hz, 2 H), 8.19 (s, 1 H), 7.87 (s, 4 H), 7.78 (d, J= 8.28 Hz, 2 H), phenyl triazole Phenyl [M]⁺ 5.63 (d, J = 1.85 Hz, 1 H),3.78 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3 H), 3.57(s, 3 H), 3.56 (s, 3 H), 3.42 (dd, J = 9.31, 3.36 Hz, 1 H), 3.18 (t, J =9.48 Hz, 1 H), 1.29 (d, J = 6.26 Hz, 3 H) 88 4-OC₂F₄H 1,3 1,2,4- 1,4 A568.0 8.59 (s, 1 H), 8.22 (d, J = 8.26 Hz, 2 H), 8.19 (s, 1 H), 7.81 (d,J = 8.22 Hz, 2 H), 7.76 (d, J = phenyl triazole Phenyl [M]⁺ 8.26 Hz, 2H), 7.41 (d, J = 8.22 Hz, 2 H), 5.97 (tt, J = 52.72, 2.64 Hz, 1 H), 5.63(d, J = 1.85 Hz, 1 H), 3.68 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H),3.59 (s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.36Hz, 1 H), 3.20 (t, J = 9.48 Hz, 1 H), 1.25 (d, J = 6.26 Hz, 3 H) 894-OC₂F₅ 1,3 1,2,4- 1,4 A 586.0 8.59 (s, 1 H), 8.21 (d, J = 8.28 Hz, 2H), 8.18 (s, 1 H), 7.81 (d, J = 8.22 Hz, 2 H), 7.77 (d, J = phenyltriazole Phenyl [M]⁺ 8.28 Hz, 2 H), 7.39 (d, J = 8.22 Hz, 2 H), 5.63 (d,J = 1.85 Hz, 1 H), 3.79 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H),3.59 (s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.43 (dd, J = 9.31, 3.36Hz, 1 H), 3.18 (t, J = 9.48 Hz, 1 H), 1.30 (d, J = 6.26 Hz, 3 H) 904-SCH₃ 1,3 1,2,4- 1,4 A 498.0 8.57 (s, 1 H), 8.21 (d, J = 8.24 Hz, 2 H),8.17 (s, 1 H), 7.73 (d, J = 8.24 Hz, 2 H), 7.64 (d, J = phenyl triazolePhenyl [M]⁺ 8.23 Hz, 2 H), 7.38 (d, J = 8.23 Hz, 2 H), 5.63 (d, J = 1.85Hz, 1 H), 3.70 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.42 (dd, J = 9.31, 3.36 Hz, 1 H),3.18 (t, J = 9.48 Hz, 1 H), 2.56 (s, 3 H), 1.28 (d, J = 6.26 Hz, 3 H) 913-OCF₃ 1,3 1,2,4- 1,4 A 536.0 8.62 (s, 1 H), 8.25 (d, J = 8.28 Hz, 2 H),8.20 (s, 1 H), 7.78 (d, J = 8.28 Hz, 2 H), 7.73 (m, 2 H), phenyltriazole Phenyl [M]⁺ 7.58 (t, J = 9.54, 1 H), 7.26 (s, 1 H), 5.63 (d, J= 1.85 Hz, 1 H), 3.72 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59(s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1H), 3.17 (t, J = 9.48 Hz, 1 H), 1.31 (d, J = 6.26 Hz, 3 H) 92 4-OC₂F₅1,3 1,2,4- 1,4 G 628.0 8.59 (s, 1 H), 8.21 (d, J = 8.26 Hz, 2 H), 8.17(s, 1 H), 7.84 (d, J = 8.24 Hz, 2 H), 7.74 (d, J = phenyl triazolePhenyl [M]⁺ 8.24 Hz, 2 H), 7.39 (d, J = 8.34 Hz, 2 H), 5.62 (d, J = 1.92Hz, 1 H), 3.91 (dd, J = 9.16, 7.24 Hz, 1 H), 3.85 (dd, J = 3.40, 1.92Hz, 1 H), 3.69-3.49 (m, 7 H), 3.29 (t, J = 9.44 Hz, 1 H), 1.33 (d, J =6.42 Hz, 3 H), 1.26 (td, J = 7.06, 3.66 Hz, 6 H), 1.18 (t, J = 7.20 Hz,3 H) 93 4-OC₂F₅ 1,3 1,2,4- 1,4 B 600.0 107 8.58 (s, 1 H), 8.21 (d, J =8.40 Hz, 2 H), 8.16 (s, 1 H), 7.79 (d, J = 8.24 Hz, 2 H), 7.72 (d, J =phenyl triazole Phenyl [M]⁺ 8.40 Hz, 2 H), 7.38 (d, J = 8.24 Hz, 2 H),5.63 (d, J = 1.85 Hz, 1 H), 3.79-3.61 (m, 4 H), 3.57 (s, 3 H), 3.56 (s,3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1 H), 3.18 (t, J = 9.48 Hz, 1 H),1.36-1.23 (m, 6 H) 95 4-CF₃ 3,5 1,2,4- 1,4 A 520.0 8.21 (d, J = 8.41 Hz,2 H), 8.13 (s, 1 H), 8.06 (d, J = 8.41 Hz, 2 H), 7.69 (d, J = 7.96 Hz, 2H), phenyl triazole Phenyl [M]⁺ 7.62 (d, J = 7.96 Hz, 2 H), 7.59 (s, 1H), 5.63 (d, J = 1.85 Hz, 1 H), 3.78 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63(m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J =9.31, 3.36 Hz, 1 H), 3.18 (t, J = 9.48 Hz, 1 H), 1.29 (d, J = 6.26 Hz, 3H) 96 4-Cl 3,5 1,2,4- 1,4 A 486.0 8.17 (s, 1 H), 8.08 (d, J = 8.22 Hz, 2H), 7.99 (d, J = 8.45 Hz, 2 H), 7.69 (d, J = 8.22 Hz, 2 H), phenyltriazole Phenyl [M]⁺ 7.61 (s, 1 H), 7.41 (d, J = 8.45 Hz, 2 H), 5.63 (d,J = 1.85 Hz, 1 H), 3.71 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H),3.59 (s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.36Hz, 1 H), 3.20 (t, J = 9.48 Hz, 1 H), 1.31 (d, J = 6.26 Hz, 3 H) 974-t-Bu 3,5 1,2,4- 1,4 A 508.0 8.15 (s, 1 H), 8.13 (d, J = 8.34 Hz, 2 H),7.93 (d, J = 8.32 Hz, 2 H), 7.62 (d, J = 8.32 Hz, 2 H), phenyl triazolePhenyl [M]⁺ 7.59 (s, 1 H), 7.41 (d, J = 8.34 Hz, 2 H), 5.63 (d, J = 1.85Hz, 1 H), 3.71 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1 H),3.20 (t, J = 9.48 Hz, 1 H), 1.29 (s, 9 H), 1.29 (d, J = 6.26 Hz, 3 H) 983,4-Cl₂ 2,5 1,2,4- 1,4 A 537 8.19 (d, J = 3.36 Hz, 1 H), 8.16 (s, 1 H),7.94 (d, J = 3.36 Hz, 1 H), 7.79 (d, J = 8.42 Hz, 2 H), phenyltriazolin-3- Phenyl [M]⁺ 7.69 (d, J = 8.42 Hz, 2 H), 7.45 (s, 1 H), 5.63(d, J = 1.85 Hz, 1 H), 3.74 (dd, J = 3.28, 1.99 Hz, one 1 H), 3.63 (m, 1H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31,3.36 Hz, 1 H), 3.18 (t, J = 9.48 Hz, 1 H), 1.27 (d, J = 6.26 Hz, 3 H) 99Perfluoro- 2,5 1,2,4- 1,4 A 608 8.16 (s, 1 H), 7.84 (d, J = 8.23 Hz, 2H), 7.75 (d, J = 8.23 Hz, 2 H), 5.63 (d, J = 1.85 Hz, 1 H), 4-tolyltriazolin-3- Phenyl [M]⁺ 3.73 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 one (dd, J = 9.31,3.36 Hz, 1 H), 3.21 (t, J = 9.48 Hz, 1 H), 1.27 (d, J = 6.26 Hz, 3 H)100 2,4-F₂ 2,5 1,2,4- 1,4 A 504 8.14 (s, 1 H), 7.86 (d, J = 8.26 Hz, 2H), 7.67 (d, J = 8.26 Hz, 2 H), 7.58 (m, 1 H), 7.03 (m, 2 H), phenyltriazolin-3- Phenyl [M]⁺ 5.63 (d, J = 1.85 Hz, 1 H), 3.77 (dd, J = 3.28,1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3 H), 3.57 one (s, 3 H), 3.56 (s,3 H), 3.41 (dd, J = 9.31, 3.36 Hz, 1 H), 3.21 (t, J = 9.48 Hz, 1 H),1.31 (d, J = 6.26 Hz, 3 H) 101 4-OCF₃ 2,5 1,2,4- 1,4 A 552 8.09 (s, 1H), 8.02 (d, J = 8.21 Hz, 2 H), 7.88 (d, J = 8.44 Hz, 2 H), 7.63 (d, J =8.44 Hz, 2 H), phenyl triazolin-3- Phenyl [M]⁺ 7.24 (d, J = 8.21 Hz, 2H), 5.63 (d, J = 1.85 Hz, 1 H), 3.72 (dd, J = 3.2, 1.99 Hz, 1 H), 3.63(m, one 1 H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.41 (dd, J =9.31, 3.36 Hz, 1 H), 3.20 (t, J = 9.48 Hz, 1 H), 1.30 (d, J = 6.26 Hz, 3H) 102 4-Br 1,3 1,2,4- 1,4 A 531.0 8.59 (s, 1 H), 8.21 (d, J = 8.26 Hz,2 H), 8.18 (s, 1 H), 7.72 (d, J = 8.26 Hz, 2 H), 7.69 (s, 4 H), phenyltriazole Phenyl [M]⁺ 5.63 (d, J = 1.85 Hz, 1 H), 3.73 (dd, J = 3.28,1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.56 (s, 3H), 3.41 (dd, J = 9.31, 3.36 Hz, 1 H), 3.19 (t, J = 9.48 Hz, 1 H), 1.28(d, J = 6.26 Hz, 3 H) 105 4-SC₂F₅ 1,3 1,2,4- 1,4 A 602.0 8.65 (s, 1 H),8.22 (d, J = 8.28 Hz, 2 H), 8.17 (s, 1 H), 7.88-7.81 (m, 4 H), 7.76 (d,J = 8.28 Hz, phenyl triazole Phenyl [M]⁺ 2 H), 5.63 (d, J = 1.85 Hz, 1H), 3.68 (dd, J = 3.28, 1.99 Hz, 1 H), 3.63 (m, 1 H), 3.59 (s, 3 H),3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1 H), 3.20(t, J = 9.48 Hz, 1 H), 1.25 (d, J = 6.26 Hz, 3 H) 106 4-OC₂F₅ 1,3 1,2,4-1,4 C 614.0 8.59 (s, 1 H), 8.20 (d, J = 8.38 Hz, 2 H), 8.18 (s, 1 H),7.79 (d, J = 8.24 Hz, 2 H), 7.75 (d, J = phenyl triazole Phenyl [M]⁺8.38 Hz, 2 H), 7.38 (d, J = 8.24 Hz, 2 H), 5.63 (d, J = 1.85 Hz, 1 H),3.71-3.62 (m, 4 H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.44 (dd, J = 9.31,3.36 Hz, 1 H), 3.20 (t, J = 9.48 Hz, 1 H), 1.68 (m, 2 H), 1.31 (d, J =6.26 Hz, 3 H), 0.98 (t, J = 7.88 Hz, 3 H) 107 4-CF₃ 1,3 1,2,4- 1,4 C549.0 188- 8.69 (s, 1 H), 8.25 (d, J = 8.7 Hz, 2 H), 8.20 (s, 1 H), 7.93(d, J = 8.4 Hz, 2 H), 7.82 (d, J = 8.7 phenyl triazole Phenyl [M + H]⁺190 Hz, 2 H), 7.76 (d, J = 8.4 Hz, 2 H), 5.67 (d, J = 2.1 Hz, 1 H),3.8-3.65 (m, 2 H), 3.65 (s, 3 H), 3.58 (s, 3 H), 3.6 (m, 3 H), 3.25 (t,J = 9.3 Hz, 1 H), 1.7 (m, 2 H), 1.33 (d, J = 6.3 Hz, 3 H), 1.01 (t, J =7.5 Hz, 3 H) 108 4-C₂F₅ 1,3 1,2,4- 1,4 C 598.0 8.62 (s, 1 H), 8.27 (d, J= 8.26 Hz, 2 H), 8.20 (s, 1 H), 7.94 (d, J = 8.33 Hz, 2 H), 7.78 (d, J =phenyl triazole Phenyl [M]⁺ 8.33 Hz, 2 H), 7.70 (d, J = 8.26 Hz, 2 H),5.62 (d, =1.85 Hz, 1 H), 3.87-3.62 (m, 4 H), 3.59 (s, 3 H), 3.56 (s, 3H), 3.46 (dd, J = 9.32, 3.34 Hz, 1 H), 3.14 (t, J = 9.46 Hz, 1 H),1.65-1.62 (m, 2 H), 1.26 (d, J = 6.10 Hz, 3 H), 0.99 (t, J = 7.62 Hz, 3H) 109 4-OC₂F₅ 1,3 1,2,4- 1,4 D 651.1 128 8.61 (s, 1 H), 8.23 (d, J =8.4 Hz, 2 H), 8.21 (s, 1 H), 7.79 (d, J = 8.2 Hz, 2 H), 7.75 (d, J = 8.4phenyl triazole Phenyl [M + Na]⁺ Hz, 2 H), 7.38 (d, J = 8.2 Hz, 2 H),5.67 (d, J = 1.85 Hz, 1 H), 3.71-3.62 (m, 5 H), 3.59 (s, 3 H), 3.57 (s,3 H), 3.20 (t, J = 9.5 Hz, 1 H), 1.68 (m, 2 H), 1.45 (m, 2 H), 1.33 (d,J = 7 Hz, 3 H), 0.98 (t, J = 7.9 Hz, 3 H) 110 4-C₃F₇ 1,3 1,2,4- 1,4 C648.0 126 8.71 (s, 1 H), 8.23 (d, J = 8.30 Hz, 2 H), 8.19 (s, 1 H), 7.94(d, J = 8.28 Hz, 2 H), 7.78-7.69 (m, phenyl triazole Phenyl [M]⁺ 4 H),5.62 (d, J = 1.85 Hz, 1 H), 3.87-3.62 (m, 4 H), 3.59 (s, 3 H), 3.56 (s,3 H), 3.46 (dd, J = 9.32, 3.34 Hz, 1 H), 3.14 (t, J = 9.46 Hz, 1 H),1.65-1.62 (m, 2 H), 1.26 (d, J = 6.10 Hz, 3 H), 0.99 (t, J = 7.62 Hz, 3H) 111 4-OC₂F₅ 1,3 1,2,4- 1,4 B 573.0 134- 8.59 (s, 1 H), 8.23 (d, J =8.7 Hz, 2 H), 8.20 (s, 1 H), 7.79 (d, J = 9.3 Hz, 2 H), 7.75 (d, J = 8.7phenyl triazole Phenyl [M]⁺ 137 Hz, 2 H), 7.39 (d, J = 9.3 Hz, 2 H),5.71 (d, J = 1.8 Hz, 1 H), 3.82 (m, 1 H), 3.77 (m, 1 H), 3.63 (m, 1 H),3.55 (s, 3 H), 3.51 (s, 3 H), 3.45 (m, 1 H), 2.4 (s, 1 H), 1.33 (d, J =7 Hz, 3 H) 112 4- 1,3 1,2,4- 1,4 B 614.0 8.61 (s, 1 H), 8.22 (d, J =8.34 Hz, 2 H), 8.19 (s, 1 H), 7.91 (d, J = 8.30 Hz, 2 H), 7.74 (d, J =CF₃SO₂O- triazole Phenyl [M]⁺ 8.30 Hz, 2 H), 7.48 (d, J = 8.34 Hz, 2 H),5.63 (d, J = 1.85 Hz, 1 H), 3.79-3.61 (m, 4 H), 3.57 (s, phenyl 3 H),3.56 (s, 3 H), 3.44 (dd, J = 9.31/3.36 Hz, 1 H), 3.18 (t, J = 9.48 Hz, 1H), 1.36-1.23 (m, 6 H) 114 4-OC₂F₅ 1,3 1,2,4- 1,4 H 617.0 8.61 (s, 1 H),8.27 (s, 1 H), 8.23 (d, J = 8.4 Hz, 2 H), 7.82 (d, J = 8.2 Hz, 2 H),7.75 (d, J = 8.4 phenyl triazole Phenyl [M]⁺ Hz, 2 H), 7.42 (d, J = 8.2Hz, 2 H), 5.80 (d, J = 3 Hz, 1 H), 3.68-3.30 (m, 18 H) 115 2-Cl, 4- 1,31,2,4- 1,4 B 568.0  94 8.69 (s, 1 H), 8.20 (d, J = 8.26 Hz, 2 H), 8.16(s, 1 H), 7.91-7.86 (m, 3 H), 7.71 (d, J = 8.26 Hz, CF₃ triazole Phenyl[M]⁺ 2 H), 5.63 (d, J = 1.85 Hz, 1 H), 3.79-3.61 (m, 4 H), 3.57 (s, 3H), 3.56 (s, 3 H), 3.44 (dd, J = phenyl 9.31, 3.36 Hz, 1 H), 3.18 (t, J= 9.48 Hz, 1 H), 1.36-1.23 (m, 6 H) 116 5-CF₃ 1,3 1,2,4- 1,4 B 535.0 1949.23 (s, 1 H), 8.78 (s, 1 H), 8.29 (d, J = 8.31 Hz, 2 H), 8.24 (s, 1 H),8.18-8.16 (m, 2 H), 7.78 (d, pyrid-2-yl triazole Phenyl [M]⁺ J = 8.31Hz, 2 H), 5.63 (d, J = 1.85 Hz, 1 H), 3.79-3.61 (m, 4 H), 3.57 (s, 3 H),3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1 H), 3.18 (t, J = 9.48 Hz,1 H), 1.36-1.23 (m, 6 H) 117 6-Cl- 1,3 1,2,4- 1,4 B 502.0 9.39 (s, 1 H),8.26 (d, J = 8.28 Hz, 2 H), 8.19-8.16 (m, 3 H), 7.78 (d, J = 8.28 Hz, 2H), 5.63 (d, pyridazin- triazole Phenyl [M]⁺ J = 1.85 Hz, 1 H),3.79-3.61 (m, 4 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31,3.36 Hz, 3-yl 1 H), 3.18 (t, J = 9.48 Hz, 1 H), 1.36-1.23 (m, 6 H) 1185-CF₃-- 1,3 1,2,4- 1,4 C 549.0 204 9.21 (s, 1 H), 8.76 (s, 1 H), 8.25(d, J = 8.34 Hz, 2 H), 8.17 (s, 1 H), 8.15-8.08 (m, 2 H), 7.75 (d,pyrid-2-yl triazole Phenyl [M]⁺ J = 8.34 Hz, 2 H), 5.62 (d, J = 1.85 Hz,1 H), 3.87-3.62 (m, 4 H), 3.59 (s, 3 H), 3.56 (s, 3 H), 3.46 (dd, J =9.32, 3.34 Hz, 1 H), 3.14 (t, J = 9.46 Hz, 1 H), 1.65-1.62 (m, 2 H),1.26 (d, J = 6.10 Hz, 3 H), 0.99 (t, J = 7.62 Hz, 3 H) 119 4-OC₂F₅ 1,31,2,4- 1,4 I 616.9 8.61 (s, 1 H), 8.24 (d, J = 8.4 Hz, 2 H), 8.21 (s, 1H), 7.79 (d, J = 8.2 Hz, 2 H), 7.75 (d, J = 8.4 phenyl triazole Phenyl[M]⁺ Hz, 2 H), 7.42 (d, J = 8.2 Hz, 2 H), 5.77 (d, J = 1.7 Hz, 1 H),3.79 (m, 1 H), 3.70 (m, 1 H), 3.61 (m, 2 H), 3.6-3.5 (m, 11 H), 3.40 (s,3 H) 120 4-OCF₃ 1,3 1,2,4- 1,4 B 551 131- 8.60 (s, 1 H), 8.24 (d, J =8.4 Hz, 2 H), 8.21 (s, 1 H), 7.83 (d, J = 8.7 Hz, 2 H), 7.77 (d, J = 8.4phenyl triazole Phenyl [M + H]⁺ 134 Hz, 2 H), 7.39 (d, J = 8.7 Hz, 2 H),5.63 (d, J = 1.6 Hz, 1 H), 3.78 -3.5 (m, 5 H), 3.61 (s, 3 H), 3.58 (s, 3H), 3.22 (t, J = 9.2 Hz, 1 H), 1.3 (m, 6 H) 121 6-CF₃ 1,3 1,2,4- 1,4 B535 217- 9.21 (s, 1 H), 8.78 (s, 1 H), 8.36 (d, J = 8.20 Hz, 1 H), 8.22(d, J = 8.26 Hz, 2 H), 8.19 (s, 1 H), pyrid-3-yl triazole Phenyl [M +H]⁺ 219 7.90 (d, J = 8.20 Hz, 1 H), 7.78 (d, J = 8.26 Hz, 2 H), 5.63 (d,J = 1.85 Hz, 1 H), 3.79-3.61 (m, 4 H), 3.57 (s, 3 H), 3.56 (s, 3 H),3.44 (dd, J = 9.31, 3.36 Hz, 1 H), 3.18 (t, J = 9.48 Hz, 1 H), 1.36-1.23(m, 6 H) 122 4-OC₂F₅ 1,3 1,2,4- 1,4 J 586.9 100- 8.58 (s, 1 H), 8.25 (s,1 H), 8.19 (d, J = 8.7 Hz, 2 H), 7.8 (m, 4 H), 7.4 (d, J = 8 Hz, 2 H),5.78 phenyl triazole Phenyl [M]⁺ 108 (d, J = 4.2 Hz, 1 H), 4.0 (m, 1 H),3.8 (m, 1 H), 3.65-3.45 (m, 11 H), 1.28 (d, J = 6.3 Hz, 3 H) 123 4-OCF₃1,3 1,2,4- 5,2- B 551 9.41 (s, 1 H), 8.60 (s, 1 H), 8.46 (d, J = 8.18Hz, 1 H), 8.32 (s, 1 H), 8.08 (d, J = 8.18 Hz, 1 H), phenyl triazolepyridyl [M + H]⁺ 7.78 (d, J = 8.22 H, 2 H), 7.41 (d, J = 8.22 Hz, 2 H),5.63 (d, J = 1.85 Hz, 1 H), 3.79-3.61 (m, 4 H), 3.57 (s, 3 H), 3.56 (s,3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1 H), 3.18 (t, J = 9.48 Hz, 1 H),1.36-1.23 (m, 6 H) 124 4- 1,3 1,2,4- 1,4 B 661 8.59 (s, 1 H), 8.21 (d, J= 8.28 Hz, 2 H), 8.18 (s, 1 H), 7.78 (d, J = 8.30 Hz, 2 H), 7.72 (d, J =OCF₂CF₂Br triazole Phenyl [M + H]⁺ 8.28 Hz, 2 H), 7.38 (d, J = 8.30 Hz,2 H), 5.63 (d, J = 1.85 Hz, 1 H), 3.79-3.61 (m, 4 H), 3.57 (s, phenyl 3H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1 H), 3.18 (t, J = 9.48Hz, 1 H), 1.36-1.23 (m, 6 H) 125 4- 1,3 1,2,4- 1,4 B 510 136- 8.46 (s, 1H), 8.24 (d, J = 8.26 Hz, 2 H), 8.18 (s, 1 H), 7.74 (d, J = 8.26 Hz, 2H), 7.62 (d, J = OCH₂CH₃ triazole Phenyl [M + H]⁺ 138 8.22 Hz, 2 H),7.04 (d, J = 8.22 Hz, 2 H), 5.63 (d, J = 1.85 Hz, 1 H), 4.12 (q, 7.22Hz, 2 H), phenyl 3.79-3.61 (m, 4 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44(dd, J = 9.31, 3.36 Hz, 1 H), 3.18 (t, J = 9.48 Hz, 1 H),1.48 (t, J =9.46 Hz, 3 H), 1.36-1.23 (m, 6 H) 126 4-CN 1,3 1,2,4- 1,4 B 491 8.72 (s,1 H), 8.24 (s, 1 H), 8.21 (d, J = 8.28 Hz, 2 H), 7.96 (d, J = 8.22 Hz, 2H), 7.82 (d, J = phenyl triazole Phenyl [M + H]⁺ 8.28 Hz, 2 H), 7.78 (d,J = 8.22 Hz, 2 H), 5.63 (d, J = 1.85 Hz, 1 H), 3.79-3.61 (m, 4 H), 3.57(s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1 H), 3.18 (t, J =9.48 Hz, 1 H), 1.36-1.23 (m, 6 H) 127 4-NO₂ 1,3 1,2,4- 1,4 B 511 178-8.79 (s, 1 H), 8.44 (d, J = 8.20 Hz, 2 H), 8.22 (d, J = 8.22 Hz, 2 H),8.18 (s, 1 H), 8.02 (d, J = phenyl triazole Phenyl [M + H]⁺ 180 8.20 Hz,2 H), 7.78 (d, J = 8.22 Hz, 2 H), 5.63 (d, J = 1.85 Hz, 1 H), 3.79-3.61(m, 4 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31, 3.36 Hz, 1H), 3.18 (t, J = 9.48 Hz, 1 H), 1.36-1.23 (m, 6 H) 128 4-OCF₃ 3,5 1,2,4-1,4 B 567 146- 8.44 (d, J = 8.20 Hz, 2 H), 8.20 (s, 1 H), 8.09 (d, J =8.24 Hz, 2 H), 7.79 (d, J = 8.20 Hz, 2 H), phenyl thiadiazole Phenyl[M + H]⁺ 148 7.38 (d, J = 8.24 Hz, 2 H), 5.63 (d, J = 1.85 Hz, 1 H),3.79-3.61 (m, 4 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31,3.36 Hz, 1 H), 3.18 (t, J = 9.48 Hz, 1 H), 1.36-1.23 (m, 6 H) 129 4-OCF₃5,3 1,2,4- 1,4 B 567 139- 8.42 (d, J = 8.26 Hz, 2 H), 8.20 (s, 1 H),8.12 (d, J = 8.22 Hz, 2 H), 7.78 (d, J = 8.26 Hz, 2 H), phenylthiadiazole Phenyl [M + H]⁺ 141 7.38 (d, J = 8.22 Hz, 2 H), 5.63 (d, J =1.85 Hz, 1 H), 3.79-3.61 (m, 4 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44(dd, J = 9.31, 3.36 Hz, 1 H), 3.18 (t, J = 9.48 Hz, 1 H), 1.36-1.23 (m,6 H) 130 4-OCF₃ 3,5 4,5-dihydro- 1,4 B 553 8.15 (s, 1 H), 7.78 (d, J =8.9 Hz, 2 H), 7.68 (d, J = 8.2 Hz, 2 H), 7.57 (d, J = 8.6 Hz, phenyl1,2,4- Phenyl [M]⁺ 2 H), 7.28 (d, J = 8.6 Hz, 2 H), 6.58 (d, J = 4.3 Hz,1 H), 5.62 (bs, 1 H), 4.95 (d, J = 4.3 oxadiazole Hz, 1 H), 3.80-3.50(m, 5 H), 3.58 (s, 3 H), 3.54 (s, 3 H), 3.19 (t, J = 9.6 Hz, 1 H), 1.35-1.20 (m, 6 H) 131 4-CF₃ 5,2 tetrazole 1,4 A 521 156- 8.39 (d, J = 9.0Hz, 2 H), 8.26 (d, J = 8.7 Hz, 2 H), 8.23 (s, 1 H), 7.86 (d, J = 8.9 Hz,2 H), 7.80 phenyl Phenyl [M]⁺ 158 (d, J = 8.5 Hz, 2 H), 5.70 (d, J = 1.8Hz, 1 H), 3.78 (m, 1 H), 3.69 (m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3 H),3.56 (s, 3 H), 3.52 (m, 1 H), 3.22 (t, J = 9.4 Hz, 1 H), 1.34 (d, J =6.2 Hz, 3 H) 133 4-OCF₃ 4,2 pyridine 1,4 A 546 112- 8.78 (d, J = 5.3 Hz,1 H), 8.23 (s, 1 H), 8.11 (d, J = 8.2 Hz, 2 H), 7.93 (s, 1 H), 7.78 (d,J = 8.6 phenyl Phenyl [M]⁺ 120 Hz, 2 H), 7.73 (d, J = 9.1 Hz, 2 H), 7.45(m, 1 H), 7.38 (d, J = 8.2 Hz, 2 H), 5.70 (d, J = 1.9 Hz, 1 H), 3.79 (m,1 H), 3.71 (m, 1 H), 3.60 (s, 3 H), 3.58 (s, 3 H), 3.56 (s, 3 H), 3.53(m, 1 H), 3.23 (t, J = 9.4 Hz, 1 H), 1.34 (d, J = 6.0 Hz, 3 H) 1344-OCF₃ 2,6 pyridine 1,4 A 546 8.23 (s, 1 H), 8.19 (d, J = 8.5 Hz, 2 H),7.86 (t, J = 7.9 Hz, 1 H), 7.76 (m, 3 H), 7.70 (d, J = 7.7 phenyl Phenyl[M]⁺ Hz, 1 H), 7.36 (d, J = 8.7 Hz, 2 H), 5.71 (d, J = 1.7 Hz, 1 H),3.80 (m, 1 H), 3.72 (m, 1 H), 3.61 (s, 3 H), 3.58 (s, 3 H), 3.57 (s, 3H), 3.53 (m, 1 H), 3.23 (t, J = 9.4 Hz, 1 H), 1.35 (d, J = 6.1 Hz, 3 H)135 4-OCF₃ 3,5 pyridine 1,4 A 546 8.85 (d, J = 17.1 Hz, 2 H), 8.21 (s, 1H), 8.03 (t, J = 1.9 Hz, 1 H), 7.78 (d, J = 8.5 Hz, 2 H), 7.68 phenylPhenyl [M]⁺ (d, J = 3.4 Hz, 2 H), 7.66 (d, J = 3.7 Hz, 2 H), 7.36 (d, J= 8.7 Hz, 2 H), 5.68 (d, J = 2.0 Hz, 1 H), 3.78 (m, 1 H), 3.69 (m, 1 H),3.59 (s, 3 H), 3.57 (s, 3 H), 3.55 (s, 3 H), 3.51 (d, J = 3.4 Hz, 1 H),3.21 (t, J = 9.5 Hz, 1 H), 1.33 (d, J = 6.2 Hz, 3 H) 136 4-OCF₃ 5,2pyrimidine 1,4 A 547 (in acetone) 9.27 (s, 2 H), 8.68 (d, J = 8.7 Hz, 2H), 8.42 (s, 1 H), 7.97 (d, J = 8.7 Hz, 2 H), 7.90 phenyl Phenyl [M]⁺(d, J = 8.5 Hz, 2 H), 7.55-7.47 (m, 2 H), 5.58 (d, J = 2.0 Hz, 1 H),3.83 (m, 1 H), 3.62 (m, 1 H), 3.53 (s, 3 H), 3.52 (s, 3 H), 3.47 (s, 3H), 3.46 (m, 1 H), 3.13 (t, J = 9.3 Hz, 1 H), 1.22 (d, J = 6.3 Hz, 3 H)137 4-OCF₃ 2,5 pyrimidine 1,4 A 547 (in acetone) 9.27 (s, 2 H), 8.68 (d,J = 9.3 Hz, 2 H), 8.42 (s, 1 H), 7.97 (d, J = 8.5 Hz, 2 H), phenylPhenyl [M]⁺ 7.90 (d, J = 8.4 Hz, 2 H), 7.52 (d, J = 8.4 Hz, 2 H), 5.58(d, J = 2.2 Hz, 1 H), 3.83 (m, 1 H), 3.62 (m, 1 H), 3.53 (s, 3 H), 3.52(s, 3 H), 3.47 (s, 3 H), 3.45 (m, 1 H), 3.13 (t, J = 9.3 Hz, 1 H), 1.22(d, J = 6.3 Hz, 3 H) 138 4-OCF₃ 4,2 pyrimidine 1,4 A 547 8.87 (d, J =5.3 Hz, 1 H), 8.62 (d, J = 8.5 Hz, 2 H), 8.29-8.20 (m, 3 H), 7.81 (d, J= 8.5 Hz, phenyl Phenyl [M]⁺ 2 H), 7.64 (d, J = 5.3 Hz, 1 H), 7.35 (d, J= 8.7 Hz, 2 H), 5.70 (d, J = 1.9 Hz, 1 H), 3.78 (m, 1 H), 3.69 (m, 1 H),3.59 (s, 3 H), 3.57 (s, 3 H), 3.55 (s, 3 H), 3.52 (m, 1 H), 3.22 (t, J =9.4 Hz, 1 H), 1.33 (d, J = 6.3 Hz, 3 H) 139 4-OCF₃ 2,4 pyrimidine 1,4 A547 8.88 (d, J = 5.3 Hz, 1 H), 8.60 (d, J = 8.4 Hz, 2 H), 8.27 (d, J =9.0 Hz, 2 H), 8.23 (s, 1 H), 7.78 phenyl Phenyl [M]⁺ (d, J = 8.5 Hz, 2H), 7.60 (d, J = 5.1 Hz, 1 H), 7.39 (d, J = 8.8 Hz, 2 H), 5.70 (d, J =1.8 Hz, 1 H), 3.78 (m, 1 H), 3.70 (m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3H), 3.55 (s, 3 H), 3.52 (m, 1 H), 3.22 (t, J = 9.5 Hz, 1 H), 1.33 (d, J= 6.2 Hz, 3 H) 140 4-OCF₃ 4,6 pyrimidine 1,4 A 547 9.34 (s, 1 H),8.26-8.16 (m, 5 H), 8.10 (s, 1 H), 7.81 (d, J = 8.6 Hz, 2 H), 7.41-7.36(m, 2 H), phenyl Phenyl [M]⁺ 5.70 (d, J = 1.9 Hz, 1 H), 3.78 (m, 1 H),3.69 (m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.55 (s, 3 H), 3.52 (m, 1H), 3.22 (t, J = 9.4 Hz, 1 H), 1.33 (d, J = 6.3 Hz, 3 H) 141 4-OC₂H₅ 5,2pyrimidine 1,4 A 597 9.04 (s, 2 H), 8.55 (d, J = 8.5 Hz, 2 H), 8.24 (s,1 H), 7.81 (d, J = 8.5 Hz, 2 H), 7.70 (d, J = 8.5 phenyl Phenyl [M]⁺ Hz,2 H), 7.43 (d, J = 8.52 Hz, 2 H), 5.71 (d, J = 1.9 Hz, 1 H), 3.79-3.81(m, 1 H), 3.74-3.69 (m, 1 H), 3.61 (s, 3 H), 3.59 (s, 3 H), 3.57 (s, 3H), 3.54-3.53 (m, 1 H), 3.23 (t, J = 9.3 Hz, 1 H), 1.35 (d, J = 6.3 Hz,3 H) 142 4-OC₂F₅ 5,2 pyrimidine 1,4 B 611 9.04 (s, 2 H), 8.55 (d, J =8.5 Hz, 2 H), 8.24 (s, 1 H), 7.81 (d, J = 8.5 Hz, 2 H), 7.70 (d, J = 8.7phenyl Phenyl [M]⁺ Hz, 2 H), 7.43 (d, J = 8.79 Hz, 2 H), 5.70 (d, J =1.6 Hz, 1 H), 3.82-3.64 (m, 5 H), 3.62 (s, 3 H), 3.59 (s, 3 H), 3.23 (t,J = 9.3 Hz, 1 H), 1.35-1.32 (m, 6 H) 143 3-OCF₃ 5,2 pyrimidine 1,4 Bphenyl Phenyl 144 4-OCF₃ 5,2 pyrimidine 1,4 C phenyl Phenyl 145 4-OCF₃5,2 pyrimidine 1,4 D phenyl Phenyl 146 4-OCF₃ 5,2 pyrimidine 1,3 Bphenyl Phenyl 147 2-OCF₃ 5,2 pyrimidine 1,3 B phenyl Phenyl 148 4-OCF₃5,2 pyrimidine 3-F, 1,4 B phenyl Phenyl 149 3-OCF₃ 5,2 pyrimidine 1,3 Bphenyl Phenyl 150 4-CH₃ 5,2 pyrimidine 1,4 B 223- Phenyl Phenyl 225 1514-CF₃ 5,2 pyrimidine 1,4 B 228- Phenyl Phenyl 229 152 2-CH₃ 5,2pyrimidine 1,4 B Phenyl Phenyl 153 4-F 5,2 pyrimidine 1,4 B 226- PhenylPhenyl 227 154 4-CN 5,2 pyrimidine 1,4 B 207- Phenyl Phenyl 211 1554-OCH₃ 5,2 pyrimidine 3-CH₃, B 121- phenyl 1,4 125 Phenyl 156 2-OCF₃ 5,2pyrimidine 1,4 B phenyl Phenyl 157 4-CF₃ 2,4 1,3,5-triazine 1,4 A 5329.32 (s, 1 H), 8.76 (d, J = 8.1 Hz, 2 H), 8.67 (d, J = 8.6 Hz, 2 H),8.24 (s, 1 H), 7.83 (d, J = 8.3 phenyl Phenyl [M]⁺ Hz, 4 H), 5.70 (d, J= 1.7 Hz, 1 H), 3.78 (dd, J = 2.0, 3.3 Hz, 1 H), 3.73-3.66 (m, 1 H),3.59 (s, 3 H), 3.57 (s, 3 H), 3.55 (s, 3 H), 3.49-3.51 (m, 1 H), 3.22(t, J = 9.3 Hz, 1 H), 1.33 (d, J = 6.1 Hz, 3 H) 158 4-OCF₃ 2,41,3,5-triazine 1,4 A 548 9.28 (s, 1 H), 8.71-8.64 (m, 4 H), 8.24 (s, 1H), 7.82 (d, J = 8.3 Hz, 2 H), 7.39 (d, J = 9.6 Hz, phenyl Phenyl [M]⁺ 2H), 5.70 (d, J = 1.7 Hz, 1 H), 3.78 (dd, J = 2.0, 3.3 Hz, 1 H),3.72-3.65 (m, 1 H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.55 (s, 3 H),3.53-3.50 (m, 1 H), 3.22 (t, J = 9.4 Hz, 1 H), 1.33 (d, J = 6.1 Hz, 3 H)159 4-OCF₃ 2,6 pyrazine 1,4 A 547 9.00 (d, J = 8.6 Hz 2 H), 8.23 (s, 1H), 8.21-8.18 (m, 4 H), 7.81 (d, J = 8.5 Hz, 2 H), 7.40 (d, phenylPhenyl [M]⁺ 2 H), 5.70 (d, J = 1.9 Hz, 1 H), 3.78 (m, 1 H), 3.69 (m, 1H), 3.59 (s, 3 H), 3.57 (s, 3 H), 3.55 (s, 3 H), 3.52 (m, 1 H), 3.22 (t,J = 9.4 Hz, 1 H), 1.33 (d, J = 6.3 Hz, 3 H) 160 4-OCF₃ 1,4 piperazine2,5- B 568 8.22 (s, 1 H), 8.08 (s, 1 H), 7.92 (d, J = 8.28 Hz, 1 H),7.12 (d, J = 8.22 Hz, 2 H), 6.94 (d, J = phenyl pyridyl [M + H]⁺ 8.22Hz, 2 H), 6.64 (d, J = 8.28 Hz, 1 H), 5.63 (d, J = 1.85 Hz, 1 H),3.82-3.61 (m, 8 H), 3.57 (s, 3 H), 3.56 (s, 3 H), 3.44 (dd, J = 9.31,3.36 Hz, 1 H), 3.31-3.22 (m, 4 H), 3.18 (t, J = 9.48 Hz, 1 H), 1.36-1.23(m, 6 H) 161 5-CF₃- 1,4 piperazine 1,4 B 552 8.42 (s, 1 H), 8.08 (s, 1H), 7.68 (d, J = 8.30 Hz, 1 H), 7.58 (d, J = 8.24 Hz, 2 H), 6.96 (d, J =pyrid-2- Phenyl [M + H]⁺ 8.24 Hz, 2 H), 6.68 (d, J = 8.30 Hz, 1 H), 5.63(d, J = 1.85 Hz, 1 H), 3.82-3.61 (m, 8 H), 3.57 (s, yl 3 H), 3.56 (s, 3H), 3.44 (dd, J = 9.31, 3.36 Hz, 1 H), 3.42-3.38 (m, 4 H), 3.18 (t, J =9.48 Hz, 1 H), 1.36-1.23 (m, 6 H) 162 4-OCF₃ 1,4 piperazine 1,4 C 5818.04 (s, 1 H), 7.52 (d, J = 8.22 Hz, 2 H), 7.14 (d, J = 8.28 Hz, 2 H),6.98-6.92 (m, 4 H), 5.62 (d, phenyl Phenyl [M + H]⁺ J = 1.85 Hz, 1 H),3.87-3.62 (m, 4 H), 3.59 (s, 3 H), 3.56 (s, 3 H), 3.46 (dd, J = 9.32,3.34 Hz, 1 H), 3.42-3.40 (m, 4 H), 3.38-3.34 (m, 4 H), 3.14 (t, J = 9.46Hz, 1 H), 1.65-1.62 (m, 2 H), 1.26 (d, J = 6.10 Hz, 3 H), 0.99 (t, J =7.62 Hz, 3 H) 163 4-SCH₃ 5,2 pyrimidine 1,4- B 210- 9.03 (s, 2 H), 8.53(d, J = 8.4 Hz, 2 H), 8.2 (s, 1 H), 7.79 (d, J = 8.7 Ha, 2 H), 7.48 (d,J = 8.7 phenyl phenyl 220 Hz, 2 H), 7.41 (d, J = 8.7 Hz, 2 H), 5.68 (s,1 H), 3.8-3.5 (series of s and m, 11 H), 3.22 (t, J = 9 Hz, 1 H), 2.57(s, 3 H), 1.33 (m, 6 H) ¹Het link: Positions on Het to which Ar₁ and Ar₂are attached respectively. ²Key to Sugars: see below. (Tables 4 and 6)³All NMR data measured in CDCl₃ at 300 or 400 MHz unless otherwisenoted.

TABLE 5

Het # Ar₁ link¹ Het Ar₂ Sugar² R5 MS ¹H NMR (CDCl₃)³ 164 4-OCF₃ 1,4imidazole 2,5 A CH₃ 556 Phenyl Thienyl [M + 1]⁺ 165 4-OCF₃ 1,4 imidazole1,4 A CH₃ 550 7.87(dd, J = 8.4, 1.8 Hz, 2 H), 7.85(s, 1 H), 7.75(d, J =Phenyl Phenyl [M + 1]⁺ 8.9 Hz, 2 H), 7.59(s, 1 H), 7.49(d, J = 9.0 Hz, 2H), 7.37(d, J = 8.7 Hz, 2 H), 5.72(s, 1 H), 3.81(dd, J = 3.1, 2.1 Hz, 1H), 3.71-3.67(m, 1 H), 3.59(s, 3 H), 3.56 (s, 3 H), 3.53-3.49(m, 4 H),3.24(d, J = 9.2 Hz, 1 H), 2.30(s, 3 H), 1.33(d, J = 6.0 Hz, 3 H) 1664-OCF₃ 1,4 imidazole 1,3 A CH₃ 550 8.15(s, 1 H), 7.89(d, J = 1.3 Hz, 1H), 7.85-7.84(m, Phenyl Phenyl [M + 1]⁺ 1 H), 7.65-7.63(m, 1 H), 7.60(d,J = 1.3 Hz, 1 H), 7.50 (d, J = 8.9 Hz, 2 H), 7.45-7.42(m, 1 H), 7.37(d,J = 8.9 Hz, 2 H), 5.74(d, J = 1.5 Hz, 1 H), 3.81(dd, J = 3.4, 2.0 Hz, 1H), 3.67-3.64(m, 1 H), 3.59(s, 3 H), 3.56(d, J = 2.2 Hz, 3 H), 3.53(s, 3H), 3.50(dd, J = 4.5, 1.3 Hz, 1 H), 3.22(t, J = 9.3 Hz, 1 H), 2.33(s, 3H), 1.33(d, J = 6.8 Hz, 3 H) 167 4-OCF₃ 1,4 imidazole 6-Cl, A CH₃ 585phenyl 1,3 [M + 1]⁺ Phenyl 168 4-OCF₃ 1,4 imidazole 6-F, 1,3 A CH₃ 5688.45(dd, J = 7.4, 1.9 Hz, 1 H), 7.92(s, 1 H), 7.75(dd, J = Phenyl Phenyl[M + 1]⁺ 4.0, 1.1 Hz, 1 H), 7.70-7.65(m, 1 H), 7.51(d, J = 9.0 Hz, 2 H),7.38(d, J = 9.3 Hz, 2 H), 7.16-7.09(m, 1 H), 5.73(s, 1 H), 3.80(dd, J =3.4, 2.2 Hz, 1 H), 3.70-3.68 (m, 1 H), 3.59(s, 3 H), 3.56(s, 3 H),3.50(d, J = 5.7 Hz, 3 H), 3.42(dd, J = 9.8, 3.2 Hz, 1 H), 3.21(t, J =9.4 Hz, 1 H), 2.33(s, 3 H), 1.32(d, J = 6.2 Hz, 3 H) 169 4-CF₃ 1,3triazole 1,4 A CF₃ 602 8.68(s, 1 H), 8.26(d, J = 8.30 Hz, 2 H), 7.88(d,J = Phenyl Phenyl [M + 1]⁺ 8.26 Hz, 2 H), 7.81(d, J = 8.26 Hz, 2 H),7.68(d, J = 8.30 Hz, 2 H), 5.63(d, J = 1.85 Hz, 1 H), 3.79-3.61(m, 4 H),3.57(s, 3 H), 3.56(s, 3 H), 3.44(dd, J = 9.31, 3.36 Hz, 1 H), 3.18(t, J= 9.48 Hz, 1 H), 1.36-1.23(m, 6 H); Het link: refers to atom positionson Het to which Ar₁ and Ar₂ are attached respectively. ²See Key toSugars, Table 4. ³All NMR data measured in CDCl₃ at 300 or 400 MHzunless otherwise noted.

TABLE 6

# Ar₁ Het link¹ Het Ar₂ Anomer Sugar² M.S. Mp (° C.) ¹H NMR (CDCl₃, δ)³172 3-Cl 1,3 4,5-dihydro- 1,4- α A 504.0 7.96-6.69(m, 9 H), 6.22(t, J =2.3 Hz, 1 H), 3.75-3.64(m, 3 H), 3.6-3.45(m, phenyl 1H-pyrazole phenyl[M + H]⁺ 11 H), 3.21(m, 3 H), 1.34(d, J = 6.0 Hz, 3 H) 173 4-OCF₃ 1,4imidazole 1,4- α A 552.0 7.87(d, J = 1.0 Hz, 1 H), 7.79(d, J = 8.9 Hz, 2H), 7.52-7.41(m, 5 H), 7.36(d, phenyl phenyl [M + H]⁺ J = 8.9 Hz, 2 H),6.90(s, 1 H), 6.24(d, J = 1.7 Hz, 1 H), 3.68(m, 2 H), 3.6-3.45 (m, 10H), 3.15(t, J = 9.2 Hz, 1 H), 1.36(d, J = 6.3 Hz, 3 H) 174 4-OCF₃ 1,4imidazole 1,4- β A 552 7.87(d, J = 1.3 Hz, 1 H), 7.80(d, J = 8.8 Hz, 2H), 7.53-7.43(m, 5 H), 7.39- phenyl phenyl [M + H]⁺ 7.34(m, 2 H),6.89(s, 1 H), 5.62(s, 1 H), 3.80(m, 1 H), 3.65(s, 3 H), 3.56(s, 3 H),3.52(s, 3 H), 3.37(m, 1 H), 3.28(m, 1 H), 3.19(t, J = 9.6 Hz, 1 H), 1.33(d, J = 6.2 Hz, 3 H) 175 4-OCF₃ 1,4 imidazole 1,4- α D 594.0 7.87(d, J =1.1 Hz, 1 H), 7.79(d, J = 8.7 Hz, 2 H), 7.50(d, J = 1.2 Hz, 1 H), phenylphenyl [M + H]⁺ 7.50-7.44(m, 4 H), 7.37(d, J = 8.8 Hz, 2 H), 6.77(s, 1H), 6.19(d, J = 1.8 Hz, 1 H), 3.68(m, 1 H), 3.62(m, 1 H), 3.59(s, 3 H),3.58(m, 1 H), 3.56(s, 3 H), 3.20(t, J = 9.6 Hz, 1 H), 1.69-1.59(m, 4 H),1.44(sext, J = 7.4 Hz, 2 H), 1.33 (d, J = 6.3 Hz, 3 H), 0.95(t, J = 7.4Hz, 3 H) 178 4-OCF₃ 1,3 4,5-dihydro- 1,4- α B 567 197-199 8.72(d, J =8.22 Hz, 2 H), 7.44(d, J = 8.22 Hz, 2 H), 7.16(d, J = 8.28 Hz, phenyl1H-pyrazole phenyl [M + H]⁺ 2 H), 7.08(d, J = 8.28 Hz, 2 H), 6.88(s, 1H), 6.20(d, J = 1.85 Hz, 1 H), 3.92(t, J = 9.46 Hz, 2 H), 3.79-3.61(m, 4H), 3.57(s, 3 H), 3.56(s, 3 H), 3.44(dd, J = 9.31, 3.36 Hz, 1 H),3.24-3.18(m, 3 H), 1.36-1.23(m, 6 H) 179 4-OC₂F₅ 1,3 4,5-dihydro- 1,4- αB 617 7.72(d, J = 8.28 Hz, 2 H), 7.44(d, J = 8.28 Hz, 2 H), 7.16(d, J =8.26 Hz, phenyl 1H-pyrazole phenyl [M + H]⁺ 2 H), 7.08(d, J = 8.26 Hz, 2H), 6.78(s, 1 H), 6.20(d, J = 1.85 Hz, 1 H), 3.88(t, J = 9.48 Hz, 2 H),3.79-3.61(m, 4 H), 3.57(s, 3 H), 3.56(s, 3 H), 3.44(dd, J = 9.31, 3.36Hz, 1 H), 3.34-3.20(m, 3 H), 1.36-1.23(m, 6 H) 180 4-OC₂F₅ 1,34-dimethyl- 1,4- α B 674 7.68(d, J = 8.26 Hz, 2 H), 7.44(d, J = 8.26 Hz,2 H), 7.14-7.08(m, 4 H), 6.92 phenyl aminomethyl- phenyl [M + H]⁺ (s, 1H), 6.20(d, J = 1.85 Hz, 1 H), 3.79-3.61(m, 7 H), 3.57(s, 3 H), 3.56(s,4,5-dihydro- 3 H), 3.44(dd, J = 9.31, 3.36 Hz, 1 H), 3.18(t, J = 9.48Hz, 1 H), 2.56-2.52(m, 1H-pyrazole 2 H), 2.40(s, 6 H), 1.36-1.23(m, 6 H)181 4-CF₃ 5,3 4.5-dihydro- 1,4- α B 552 — 7.45-7.63(m, 8 H), 6.94(bs, 1H), 6.17(bs, 1 H), 5.79(dd, J = 10.7, 7.6 Hz, phenyl isoxazole phenyl[M]⁺ 1 H), 3.50-3.90(m, 5 H), 3.58(s, 3 H), 3.54(s, 3 H), 3.10-3.40(m, 3H), 1.2-1.4 (m, 6 H) 182 4-CF₃ 5,3 4,5-dihydro- 1,4- β B 552 —7.40-7.70(m, 8 H), 6.98(bs, 1 H), 5.79(dd, J = 11.2, 7.9 Hz, 1 H),5.63(bs, phenyl isoxazole phenyl [M]⁺ 1 H), 3.50-3.90(m, 4 H), 3.66(s, 3H), 3.57(s, 3 H), 3.20-3.40(m, 3 H), 3.14(t, J = 9.4 Hz, 1 H),1.20-1.40(m, 6 H) 183 4-OCF₃ 3,5 4,5-dihydro- 1,4- α B 568 — 7.72(d, J =8.9 Hz, 2 H), 7520-7.20(m, 6 H), 6.74(s, 1 H), 6.16(s, 1 H), 5.73 phenylisoxazole phenyl [M]⁺ (dd, J = 11.0, 8.4 Hz, 1 H), 3.80-3.45(m, 6 H),3.58(s, 3 H), 3.54(s, 3 H), 3.30 (dd, J = 16.6, 8.4 Hz, 1 H), 3.19(t, J= 9.2 Hz, 1 H), 1.20-1.35(m, 6 H) 184 4-OCF₃ 3,5 4,5-dihydro- 1,4- β B568 — 7.72(d, J = 8.9 Hz, 2 H), 7.40(d, J = 8.6 Hz, 2 H), 7.33(d, J =8.9 Hz, 2 H) phenyl isoxazole phenyl [M]⁺ 7.26(d, J = 8.6 Hz, 2 H),6.84(s, 1 H), 5.73(dd, J = 11.2, 8.2 Hz, 1 H), 5.63 (bs, 1 H),3.55-3.80(m, 4 H), 3.66(s, 3 H), 3.57(s, 3 H), 3.20-3.40(m, 3 H),3.14(t, J = 9.2 Hz, 1 H), 1.20-1.40(m, 6 H) 185 4-OCF₃ 5,2 4,5-dihydro-1,4- α B 568 130-132 7.68(d, J = 8.22 Hz, 2 H), 7.44(d, J = 8.22 Hz, 2H), 7.22(d, J = 8.26 Hz, phenyl oxazole phenyl [M + H]⁺ 2 H), 7.16(d, J= 8.26 Hz, 2 H), 6.96(s, 1 H), 6.20(d, J = 1.85 Hz, 1 H), 3.79- 3.61(m,6 H), 3.57(s, 3 H), 3.56(s, 3 H), 3.44(dd, J = 9.31, 3.36 Hz, 1 H), 3.18(t, J = 9.48 Hz, 1 H), 2.92(t, J = 9.60 Hz, 2 H), 1.36-1.23(m, 6 H) 1864-OCF₃ 2,4 4,5-dihydro- 1,4- α B 568 137-139 8.02(d, J = 8.20 Hz, 2 H),7.52(d, J = 8.20 Hz, 2 H), 7.38(d, J = 8.24 Hz, phenyl oxazole phenyl[M + H]⁺ 2 H), 7.22(d, J = 8.24 Hz, 2 H), 6.84(s, 1 H), 6.20(d, J = 1.85Hz, 1 H), 5.44(t, J = 9.42 Hz, 1 H), 4.82(t, J = 9.48 Hz, 1 H), 4.28(t,J = 8.48 Hz, 1 H), 3.79- 3.61(m, 4 H), 3.57(s, 3 H), 3.56(s, 3 H),3.44(dd, J = 9.31, 3.36 Hz, 1 H), 3.18 (t, J = 9.48 Hz, 1 H),1.36-1.23(m, 6 H) 187 4-OCF₃ 1,3 1,3-dihydro- 1,4- α B 581 7.70(d, J =8.9 Hz, 2 H), 7.40-7.60(m, 4 H), 7.31(d, J = 8.6 Hz, 2 H), 7.03 phenylimidazol-2- phenyl [M]⁺ (bs, 1 H), 6.70(dd, J = 5.3, 3.3 Hz, 1 H),6.18(bs, 1 H), 3.50-3.80(m, 6 H), one 3.58(s, 3 H), 3.55(s, 3 H),3.19(t, J = 9.2 Hz, 1 H), 1.20-1.35(m, 6 H) 188 4-OCF₃ 1,3 imidazolidin-1,4- α B 583[M]⁺ 7.62(d, J = 8.9 Hz, 2 H), 7.53(d, J = 8.9 Hz, 2 H),7.35-7.45(m, 2 H), 7.23(d, J = 8.6 phenyl 2-one phenyl Hz, 2 H),6.69(bs, 1 H), 6.17(bs, 1 H), 3.97(s, 4 H), 3.50-3.80(m, 5 H), 3.59(s, 3H) 3.55(s, 3 H), 3.20(t, J = 9.2 Hz, 1 H), 1.20-1.35(m, 6 H) 192 4-CF₃1,3 1,2,4- 1,4- α B 551 185 8.65(s, 1 H), 8.18(d, J = 8.4 Hz, 2 H),7.91(d, J = 8.5 Hz, 2 H), 7.79(d, J = phenyl triazole phenyl [M + H]⁺9.0 Hz, 2 H), 7.54(d, J = 8.4 Hz, 2 H), 6.84(s, 1 H), 6.20(d, J = 1.7Hz, 1 H), 3.78-3.50(m, 11 H), 3.22(t, J = 9.3 Hz, 1 H), 1.33(d, J = 6.3Hz, 3 H), 1.29(t, J = 7.0 Hz, 3 H) 193 4-OCF₃ 1,3 1,2,4- 1,4- α B 566.98.56(s, 1 H), 8.16(d, J = 8.4 Hz, 2 H), 7.79(d, J = 9.1 Hz, 2 H),7.53(d, J = phenyl triazole phenyl [M + H]⁺ 8.6 Hz, 2 H), 7.38(d, J =9.1 Hz, 2 H), 6.79(s, 1 H), 6.20(d, J = 1.7 Hz, 1 H), 3.80-3.50(m, 11H), 3.21(t, J = 9.2 Hz, 1 H), 1.37-1.23(m, 6 H) 194 4-OCF₃ 1,3 5-CH₃-1,4- α A 566.9 8.10(d, J = 8.8 Hz, 2 H), 7.57(d, J = 9.3 Hz, 2 H),7.50(d, J = 7.3 Hz, 2 H), phenyl 1,2,4- phenyl [M + H]⁺ 7.38(d, J = 8.5Hz, 2 H), 6.80(s, 1 H), 6.22(d, J = 2.0 Hz, 1 H), 3.68(m, 2 H), triazole3.58(s, 3 H), 3.56(s, 3 H), 3.53(s, 3 H), 3.49(m, 1 H), 3.21(t, J = 9.5Hz, 1 H), 2.59(s, 3 H), 1.33(d, J = 6.2 Hz, 3 H) 195 4-OCF₃ 1,3 5-CH₃-1,4- β A 566.9 8.10(d, J = 8.8 Hz, 2 H), 7.57(d, J = 9.3 Hz, 2 H),7.50(d, J = 7.3 Hz, 2 H), phenyl 1,2,4- phenyl [M + H]⁺ 7.38(d, J = 8.5Hz, 2 H), 6.80(s, 1 H), 6.22(d, J = 2.0 Hz, 1 H), 3.68(m, 2 H(, triazole3.58(s, 3 H), 3.56(s, 3 H), 3.53(s, 3 H), 3.49(m, 1 H), 3.21(t, J = 9.5Hz, 1 H), 2.59(s, 3 H), 1.33(d, J = 6.2 Hz, 3 H) 196 4-O-(4- 1,3 1,2,4-1,4- α A 595.0 8.50(s, 1 H), 8.16(d, J = 9.1 Hz, 2 H), 7.69(d, J = 9.1Hz, 2 H), 7.53(d, J = ClPh)- triazole phenyl [M]⁺ 8.5 Hz, 2 H), 7.33(d,J = 8.9 Hz, 2 H), 7.12(d, J = 9.1 Hz, 2 H), 6.99(d, J = phenyl 8.9 Hz, 2H), 6.87(s, 1 H), 6.22(d, J = 2.0 Hz, 1 H), 3.70(m, 2 H), 3.58(s, 3 H),3.56(s, 3 H), 3.53(s, 3 H), 3.50(m, 1 H), 3.21(t, J = 9.4 Hz, 1 H),1.33(d, J = 6.1 Hz, 3 H) 197 4-CH₃ 3,1 1,2,4- 1,4- α D 8.58(s, 1 H),8.15(d, 2 H), 7.75(d, 2 H), 7.62(d, 2 H), 7.32(d, 2 H), 7.05(s, phenyltriazole phenyl 1 H), 6.22(d, 1 H), 3.7-3.5(m, 11 H), 3.21(t, 1 H),2.41(s, 3 H), 1.65(m, 2 H), 1.45(m, 2 H), 1.33(d, 3 H), 0.95(t, J = 7.5Hz, 3 H) 198 4-CF₃ 3,1 1,2,4- 1,4- α D 579.0 175 8.59(s, 1 H), 8.56(d, J= 7.6 Hz, 2 H), 7.77-7.71(m, 4 H), 7.60(d, J = 8.9 Hz, phenyl triazolephenyl [M + H]⁺ 2 H), 6.90(s, 1 H), 6.20(d, J = 1.8 Hz, 1 H),3.75-3.57(m, 11 H), 3.20(t, J = 9.3 Hz, 1 H), 1.66(m, 2 H), 1.47(sext, J= 7.4 Hz, 2 H), 1.39(t, J = 6.3 Hz, 3 H), 0.98(t, J = 7.3 Hz, 3 H) 1994-CF₃ 3,1 1,2,4- 1,4- β D 579.0 179 8.59(s, 1 H), 8.34(d, J = 7.6 Hz, 2H), 7.77-7.71(m, 4 H), 7.60(d, J = 8.9 Hz, phenyl triazole phenyl [M +H]⁺ 2 H), 7.0(s, 1 H), 5.68(d, J = 0.8 Hz, 1 H), 3.80-3.78(m, 1 H),3.75-3.57(m, 8 H), 3.41(dd, J = 9.2, 6.1 Hz, 1 H), 3.37(dd, J = 9.4, 3.0Hz, 1 H), 3.18(t, J = 9.3 Hz, 1 H), 1.66(m, 2 H), 1.47(sext, J = 7.4 Hz,2 H), 1.39(d, J = 6.3 Hz, 3 H), 0.98(t, J = 7.3 Hz, 3 H) 200 4-OC₂F₅ 1,31,2,4- 1,4- α A 603.0 207-210 8.59(s, 1 H), 8.20(d, J = 8.7 Hz, 2 H),7.85(d, J = 8 Hz, 2 H), 7.5(d, J = 8 Hz, phenyl triazole phenyl [M + H]⁺2 H), 7.30(t, J = 8.7 Hz, 2 H), 6.80(s, 1 H), 6.22(d, J = 1.8 Hz, 1 H),3.65- 3.45(m, 12 H), 3.20(t, J = 9.3 Hz, 1 H), 1.33(d, J = 6.2 Hz, 3 H)204 4-OC₂F₅ 1,3 1,2,4- 1,4- α K 629.0 8.6(s, 1 H), 8.20(d, J = 8.7 Hz, 2H), 7.81(d, J = 8.7 Hz, 2 H), 7.55(d, J = 8.4 phenyl triazole phenyl[M + H]⁺ Hz, 2 H), 7.38(d, J = 8.7 Hz, 2 H), 6.95(s, 1 H), 6.21(d, J =1.8 Hz, 1 H), 6.0 (m, 1 H), 5.35(d, J = 12 Hz, 1 H), 5.21(d, J = 8 Hz, 1H), 4.20(d, J = 6 Hz, 2 H), 3.75-3.50(m, 9 H), 3.23(t, J = 9.5 Hz, 1 H),1.33(d, J = 7 Hz, 3 H) 205 4-OCF₃ 1,3 1,2,4- 1,4- α K 579.0 8.55(s, 1H), 8.17(d, J = 8.7 Hz, 2 H), 7.80(d, J = 8.7 Hz, 2 H), 7.55(d, J =phenyl triazole phenyl [M + H]⁺ 8.4 Hz, 2 H), 7.38(d, J = 8.7 Hz, 2 H),6.85(s, 1 H), 6.20(d, J = 1.8 Hz, 1 H), 6.0(m, 1 H), 5.35(d, J = 12 Hz,1 H), 5.21(d, J = 8 Hz, 1 H), 4.20(d, J = 6 Hz, 2 H), 3.75-3.50(m, 9 H),3.23(t, J = 9.5 Hz, 1 H), 1.33(d, J = 7 Hz, 3 H) 206 4-OC₂F₅ 1,3 1,2,4-1,4- α G 644.97 142-144 8.58(s, 1 H), 8.2(d, J = 8 Hz, 2 H), 7.82(d, J =8 Hz, 2 H), 7.55(d, J = 9 Hz, phenyl triazole phenyl [M + H]⁺ 2 H),7.41(d, J = 9 Hz, 2 H), 6.81(s, 1 H), 6.16(d, J = 1.5 Hz, 1 H),3.98-3.82 (m, 1 H), 3.8-3.55(m, 8 H), 3.32(t, J = 9.3 Hz, 1 H), 1.35(d,J = 6.3 Hz, 3 H), 1.3-1.11(m, 9 H) 208 4-OC₂F₅ 1,3 1,2,4- 1,4- β A 602.8— 8.6(s, 1 H), 8.2(d, J = 8 Hz, 2 H), 7.8(d, J = 8 Hz, 2 H), 7.55(d, J =9 Hz, phenyl triazole phenyl [M + H]⁺ 2 H), 7.39(d, J = 9 Hz, 2 H),6.84(s, 1 H), 6.21(d, J = 1.5 Hz, 1 H), 3.65-3.44 (m, 12 H), 3.22(t, J =9.3 Hz, 1 H), 1.35(d, J = 6.3 Hz, 3 H) 209 4-OCF₃ 1,3 1,2,4- 1,4- α C144-147 8.58(s, 1 H), 8.2(d, J = 8.6 Hz, 2 H), 7.82(d, J = 8 Hz, 2 H),7.56(d, J = 9 phenyl triazole phenyl Hz, 2 H), 7.41(d, J = 9 Hz, 2 H),6.85(s, 1 H), 6.22(d, J = 1.5 Hz, 1 H), 3.75- 3.48(m, 11 H), 3.23(t, J =9.3 Hz, 1 H), 1.69(m, 2 H), 1.35(d, J = 6.3 Hz, 3 H), 1.00(t, J = 7.5Hz, 3 H) 210 4-OCF₃ 1,3 1,2,4- 1,4- β B 566 — 8.55(s, 1 H), 8.2(d, J = 8Hz, 2 H), 7.82(d, J = 8 Hz, 2 H), 7.55(d, J = 9 Hz, phenyl triazolephenyl [M]⁺ 2 H), 7.41(d, J = 9 Hz, 2 H), 6.95(s, 1 H), 5.66(s, 1 H),3.7-3.3(m, 11 H), 3.18(t, J = 9 Hz, 1 H), 1.35(d, J = 6.3 Hz, 3 H),1.25(t, J = 7.5 Hz, 3 H) 212 4-OCF₃ 1,3 1,2,4- 1,4- α/β L 538 — 8.55(s,1 H), 8.16(d, J = 8.4 Hz, 2 H), 7.79(d, J = 8.8 Hz, 2 H), 7.53(d, J =phenyl triazole phenyl [M]⁺ 8.8 Hz, 2 H), 7.38(d, J = 8.7 Hz, 2 H), 6.94and 6.89(2 s, 1 H), 6.27(d, J = 3.7 Hz, major) and 5.56(d, J = 7.7 Hz,minor, total 1 H in a 1.6:1 α:β ratio), 4.04- 3.16(series of s and m, 14H) 213 4-OC₂F₅ 1,3 1,2,4- 1,4- α/β L 588 — 8.56(s, 1 H), 8.16(d, J = 8.8Hz, 2 H), 7.81(d, J = 9.1 Hz, 2 H), 7.54(d, J = phenyl triazole phenyl[M]⁺ 8.8 Hz, 2 H), 7.39(d, J = 9.0 Hz, 2 H), 6.95 and 6.90(br, total 1H), 6.27(d, J = 3.7 Hz, major) and 5.57(d, J = 7.5 Hz, minor, total 1 Hin a 3.8:1 α:β ratio), 4.08-2.96(series of s and m, 14 H) 214 4-OCF₃ 1,31,2,4- 1,4- α M 538 176-179 8.55(s, 1 H), 8.16(d, J = 8.4 Hz, 2 H),7.79(d, J = 9.0 Hz, 2 H), 7.53(d, J = phenyl triazole phenyl [M]⁺ 8.3Hz, 2 H), 7.38(d, J = 8.8 Hz, 2 H), 6.89(s, 1 H), 6.15(d, J = 3.4 Hz, 1H), 4.00-3.93(m, 1 H), 3.69-3.39(series of s and m, 13 H) 215 4-OCF₃ 1,31,2,4- 1,4- β M 538 77-80 8.54(s, 1 H), 8.14(d, J = 9.0 Hz, 2 H),7.79(d, J = 9.0 Hz, 2 H), 7.54(d, J = phenyl triazole phenyl [M]⁺ 9.0Hz, 2 H), 7.37(d, J = 9.1 Hz, 2 H), 7.08(br, 1 H), 6.19(d, J = 3.1 Hz, 1H), 4.05(dd, J = 12.8, 1.7 Hz, 1 H), 3.74(t, J = 3.5 Hz, 1 H),3.72-3.66(m, 2 H), 3.57-3.51(2 s and m, 7 H), 3.46(s, 3 H) 216 4-OC₃F₇1,3 1,2,4- 1,4- α C 681.12 8.7(s, 1 H), 8.2(d, J = 8 Hz, 2 H), 7.83(d, J= 8 Hz, 2 H), 7.55(d, J = 9 Hz, phenyl triazole phenyl [M + H]⁺ 2 H),7.41(d, J = 9 Hz, 2 H), 6.93(s, 1 H), 6.21(br s, 1 H), 3.7-3.44(m, 11H), 3.23(t, J = 9.3 Hz, 1 H), 1.71(m, 2 H), 1.35(d, J = 6.3 Hz, 3 H),0.98(t, J = 7.5 Hz, 3 H) 217 4-OC₂F₅ 1,3 1,2,4- 1,4- α O 633 71-818.57(s, 1 H), 8.15(d, J = 8.7 Hz, 2 H), 7.80(d, J = 9.0 Hz, 2 H),7.53(d, J = phenyl triazole phenyl [M + H]⁺ 8.5 Hz, 2 H), 7.38(d, J =8.9 Hz, 2 H), 6.97(s, 1 H), 6.35(d, J = 4.0 Hz, 1 H), 3.78-3.46(m, 13H), 3.42-3.16(m, 5 H) 218 4-OCF₃ 1,3 5-vinyl- 1,4- α β 592 8.18(d, J =8.20 Hz, 2 H), 7.58(d, J = 8.24 Hz, 2 H), 7.52(d, J = 8.20 Hz, phenyl1,2,4- phenyl [M]⁺ 2 H), 7.40(d, J = 8.24 Hz, 2 H), 6.78(s, 1 H),7.62-7.58(m, 2 H), 6.20(d, J = triazole 1.85 Hz, 1 H), 7.78-7.72(m, 1H), 3.79-3.61(m, 4 H), 3.57(s, 3 H), 3.56(s, 3 H), 3.44(dd, J = 9.31,3.36 Hz, 1 H), 3.18(t, J = 9.48 Hz, 1 H), 1.36-1.23(m, 6 H) 219 4-OCF₃1,3 5-isobutyl- 1,4- α B 622 8.08(d, J = 8.28 Hz, 2 H), 7.58-7.48(m, 4H), 7.38(d, J = 8.28 Hz, 2 H), 7.06 phenyl 1,2,4- phenyl [M]⁺ (s, 1 H),6.20(d, J = 1.85 Hz, 1 H), 3.79-3.61(m, 4 H), 3.57(s, 3 H), 3.56(s,triazole 3 H), 3.44(dd, J = 9.31, 3.36 Hz, 1 H), 3.18(t, J = 9.48 Hz, 1H), 2.68(d, J = 6.32 Hz, 2 H), 2.24-2.18(m, 1 H), 1.36-1.23(m, 6 H),0.98-0.90(m, 6 H) 220 4-OCF₃ 1,3 5-propen-2- 1,4- α B 606 8.14(d, J =8.24 Hz, 2 H), 7.58(d, J = 8.28 Hz, 2 H), 7.52(d, J = 8.24 Hz, phenylyl)-1,2,4- phenyl [M ]⁺ 2 H), 7.38(d, J = 8.28 Hz, 2 H), 6.88(s, 1 H),6.20(d, J = 1.85 Hz, 1 H), 5.44 triazole (s, 1 H), 5.32(s, 1 H),3.79-3.61(m, 4 H), 3.57(s, 3 H), 3.56(s, 3 H), 3.44(dd, J = 9.31, 3.36Hz, 1 H), 3.18(t, J = 9.48 Hz, 1 H), 2.08(s, 3 H), 1.36-1.23(m, 6 H) 2214-OCF₃ 1,3 5- 1,4- α B 640 8.08(d, J = 8.22 Hz, 2 H), 7.60(d, J = 8.26Hz, 2 H), 7.52(d, J = 8.22 Hz, phenyl (methylthio- phenyl [M]⁺ 2 H),7.42(d, J = 8.26 Hz, 2 H), 6.92(s, 1 H), 6.20(d, J = 1.85 Hz, 1 H),3.79- ethyl)- 3.61(m, 4 H), 3.57(s, 3 H), 3.56(s, 3 H), 3.44(dd, J =9.31, 3.36 Hz, 1 H), 1,2,4- 3.22-3.08(m, 3 H), 2.98(t, J = 9.42 Hz, 2H), 2.04(s, 3 H), 1.36-1.23(m, 6 H) triazole 222 4-OCF₃ 1,3 5-trifluoro-1,4- α B 634 8.12(d, J = 8.28 Hz, 2 H), 7.58(d, J = 8.28 Hz, 2 H),7.52(d, J = 8.28 Hz, phenyl methyl- phenyl [M]⁺ 2 H), 7.42(d, J = 8.28Hz, 2 H), 6.84(s, 1 H), 6.20(d, J = 1.85 Hz, 1 H), 3.79- 1,2,4- 3.61(m,4 H), 3.57(s, 3 H), 3.56(s, 3 H), 3.44(dd, J = 9.31, 3.36 Hz, 1 H), 3.18triazole (t, J = 9.48 Hz, 1 H), 1.36-1.23(m, 6 H) 223 4-OCF₃ 1,3 1,2,4-2-Br, α B 645 8.58(s, 1 H), 8.38(s, 1 H), 8.32(d, J = 8.30 Hz, 1 H),8.18(d, J = 8.30 Hz, phenyl triazole 1,4- [M]⁺ 1 H), 7.80(d, J = 8.22Hz, 2 H), 7.42(d, J = 8.22 Hz, 2 H), 7.28(s, 1 H), 6.20 phenyl (d, J =1.85 Hz, 1 H), 3.79-3.61(m, 4 H), 3.57(s, 3 H), 3.56(s, 3 H), 3.44(dd, J= 9.31, 3.36 Hz, 1 H), 3.18(t, J = 9.48 Hz, 1 H), 1.36-1.23(m, 6 H) 2244-OC₂F₅ 1,3 1,2,4- 2-Br, α B 695 8.56(s, 1 H), 8.38(s, 1 H), 8.36(d, J =8.26 Hz, 1 H), 8.18(d, J = 8.26 Hz, phenyl tirazole 1,4- [M]⁺ 1 H),7.82(d, J = 8.28 Hz, 2 H), 7.42(d, J = 8.28 Hz, 2 H), 7.28(s, 1 H), 6.20phenyl (d, J = 1.85 Hz, 1 H), 3.79-3.61(m, 4 H), 3.57(s, 3 H), 3.56(s, 3H), 3.44(dd, J = 9.31, 3.36 Hz, 1 H), 3.18(t, J = 9.48 Hz, 1 H),1.36-1.23(m, 6 H) 225 4-OC₃F₇ 1,3 1,2,4- 1,4- α B 158-162 8.59(s, 1 H),8.18(d, J = 8.7 Hz, 2 H), 7.84(d, J = 8 Hz, 2 H), 7.58(d, J = 8 phenyltriazole phenyl Hz, 2 H), 7.38(d, J = 8.7 Hz, 2 H), 6.85(s, 1 H),6.22(d, J = 1.8 Hz, 1 H), 3.65- 3.45(m, 11 H), 3.20(t, J = 9.3 Hz, 1 H),1.33(m, 6 H) 226 4-OCF₃ 2,4 5-MeO₂C— 1,4- α B 639 113-120 8.10(d, J =10.1 Hz, 2 H), 7.60-7.51(m, 2 H), 7.34-7.27(m, 4 H), 6.85(br, phenyl1,2,4- phenyl [M − H]⁺ dec 1 H), 6.18(d, J = 1.7 Hz, 0.9 H), 5.65(d, J =0.9 Hz, 0.1 H), 3.90(s, 3 H), 3.78- triazolin-3- 3.33(m, 11 H), 3.21(t,J = 9.4 Hz, 1 H), 1.38-1.25(m, 6 H) (9:1 mixture of one α:β) 227 4-OCF₃2,4 5-MeO₂C— 1,4- β B 639 122-128 8.09(d, J = 9.5 Hz, 2 H), 7.56(d, J =8.9 Hz, 2 H), 7.31(d, J = 8.7 Hz, 4 H), phenyl 1,2,4- phenyl [M − H]⁺6.94(br, 1 H), 5.65(d, J = 0.8 Hz, 1 H), 3.90(s, 3 H), 3.79-3.54(m, 9H), 3.41- triazolin-3- 3.34(m, 2 H), 3.16(t, J = 9.2 Hz, 1 H), 1.36(d, J= 6.1 Hz, 3 H), 1.29(t, J = one 7.0 Hz, 3 H) 228 4-OCF₃ 2,4 1,2,4- 1,4-α B 581 166-168 8.06(d, J = 9.0 Hz, 2 H), 7.81(s, 1 H), 7.58-7.46(m, 4H), 7.29(d, J = 8.9 Hz, phenyl triazolin-3- phenyl [M − H]⁺ 2 H),6.89(s, 1 H), 6.17(d, J = 1.8 Hz, 1 H), 3.79-3.52(m, 11 H), 3.19(t, J =one 9.3 Hz, 1 H), 1.31(d, J = 6.3 Hz, 3 H), 1.27(t, J = 7.0 Hz, 3 H) 2294-CF₃ 3.1 1,2,4- 1,4- α A 536.0 207 8.56(s, 1 H), 8.31(d, J = 8.3 Hz, 2H), 7.76-7.69(m, 4 H), 7.60(d, J = 8.4 Hz, phenyl triazole phenyl [M +H]⁺ 2 H), 6.83(s, 1 H), 6.23(d, J = 1.9 Hz, 1 H), 3.74-3.66(m, 2 H),3.59(s, 3 H), 3.57(s, 3 H), 3.54(s, 3 H), 3.50(dd, J = 9.5, 3.4 Hz, 1H), 3.22(t, J = 9.5 Hz, 1 H), 1.34(d, J = 6.2 Hz, 3 H) 230 2,4-Cl₂ 2,51,3,4- 1,4- α A 8.15(d, 1 H), 7.93(d, 2 H), 7.9(m, 1 H), 7.55(d, 2 H),7.22(d, 1 H), 8.80(br s, phenyl oxadiazole phenyl 1 H), 6.22(d, J = 1.7Hz, 1 H), 3.7-3.4(m, 12 H), 3.22(t, J = 9.3 Hz, 1 H), 1.33 (d, J = 6.3Hz, 3 H) 231 3-Cl, 4-F 2,4 thiazole 1,4- 110 8.15(m, 4 H), 7.66(d, J = 8Hz, 2 H), 7.62(d, J = 1.5 Hz, 1 H), 7.44(d, J = 8 phenyl phenyl Hz, 1H), 7.22(s, 1 H), 6.22(d, J = 1.5 Hz, 1 H), 4.8-4.5(m, 12 H), 3.2(t, J =9.3 Hz, 1 H), 1.34(d, J = 6.3 Hz, 3 H) 233 4-CF₃ 2,4 pyrimidine, 1,4- αA 715.8 8.72(d, J = 8.6 Hz, 2 H), 8.29(d, J = 8.7 Hz, 2 H), 7.93(s, 1H), 7.79(d, J = phenyl 6-(C₃F₇) phenyl [M]⁺ 8.4 Hz, 2 H), 7.66(d, J =8.6 Hz, 2 H), 6.92(s, 1 H), 6.24(d, J = 1.9 Hz, 1 H), 3.71(m, 2 H),3.59(s, 3 H), 3.58(s, 3 H), 3.55(s, 3 H), 3.51(m, 1 H), 3.23(t, J = 9.5Hz, 1 H), 1.35(d, J = 6.2 Hz, 3 H) 235 4-CF₃ 2,4 pyrimidine, 1,4- α A615.0 8.75(d, J = 8.7 Hz, 2 H), 8.3(d, J = 8.7 Hz, 2 H), 7.94(s, 1 H),7.81(d, J = 8.7 phenyl 6-(CF₃) phenyl [M]⁺ Hz, 2 H), 7.67(d, J = 8.7 Hz,2 H), 6.9(s, 1 H), 6.26(s, 1 H), 3.8-3.7(m, 1 H), 3.65-3.55(m, 11 H),3.25(t, J = 9 Hz, 1 H), 1.36(d, J = 6.3 Hz, 3 H) 236 4-OCF₃ 5,2pyrimidine 1,4- α C 591.8 9.0(s, 2 H), 8.52(d, J = 8 Hz, 2 H), 7.68(d, J= 8 Hz, 2 H), 7.60(d, J = 9 Hz, phenyl phenyl [M + H]⁺ 2 H), 7.38(d, J =9 Hz, 2 H), 6.9(s, 1 H), 6.21(br s, 1 H), 3.7-3.44(m, 11 H), 3.23(t, J =9.3 Hz, 1 H), 1.71(m, 2 H), 1.35(d, J = 6.3 Hz, 3 H), 0.98(t, J = 7.5Hz, 3 H) 237 4-OCF₃ 5,3 1,2,4- 1,4- α B 578 9.58(s, 1 H), 8.58(d, J =8.26 Hz, 2 H), 8.32(d, J = 8.24 Hz, 2 H), 7.62(d, J = phenyl triazinephenyl [M]⁺ 8.26 Hz, 2 H), 7.38(d, J = 8.24 Hz, 2 H), 7.08(s, 1 H),6.20(d, J = 1.85 Hz, 1 H), 3.79-3.61(m, 4 H), 3.57(s, 3 H), 3.56(s, 3H), 3.44(dd, J = 9.31, 3.36 Hz, 1 H), 3.18(t, J = 9.48 Hz, 1 H),1.36-1.23(m, 6 H) 238 4-OCF₃ 3,5 1,2,4- 1,4- α B 578 9.58(s, 1 H),8.72(d, J = 8.22 Hz, 2 H), 8.30(d, J = 8.26 Hz, 2 H), 7.72(d, J = phenyltriazine phenyl [M]⁺ 8.22 Hz, 2 H), 7.40(d, J = 8.26 Hz, 2 H), 7.12(s, 1H), 6.20(d, J = 1.85 Hz, 1 H), 3.79-3.61(m, 4 H), 3.57(s, 3 H), 3.56(s,3 H), 3.44(dd, J = 9.31, 3.36 Hz, 1 H), 3.18(t, J = 9.48 Hz, 1 H),1.36-1.23(m, 6 H) 239 4-OCF₃ 5.2 pyridine 1,4- α B phenyl phenyl 2404-OCF₃ 5.3 1,2,4- 1,4- α B 567 8.27(d, J = 8.9 Hz, 2 H), 8.14(d, J = 8.6Hz, 2 H), 7.58(d, J = 8.6 Hz, 2 H), phenyl oxadiazole phenyl [M]⁺7.39(d, J = 8.6 Hz, 2 H), 6.88(s, 1 H), 6.20(s, 1 H), 3.50-3.80(m, 11H), 3.21 (t, J = 9.6 Hz, 1 H), 1.33(d, J = 6.3 Hz, 3 H), 1.29(t, J = 6.9Hz, 3 H) 241 4-OCF₃ 1,4 piperazine 1,4- α B 583 155-157 7.38(d, J = 8.24Hz, 2 H), 7.16(d, J = 8.30 Hz, 2 H), 6.98-6.89(m, 4 H), 6.62 phenylphenyl [M]⁺ (s, 1 H), 6.20(d, J = 1.85 Hz, 1 H), 3.79-3.61(m, 4 H),3.57(s, 3 H), 3.56(s, 3 H), 3.39-3.18(m, 9 H), 3.18(t, J = 9.48 Hz, 1H), 1.36-1.23(m, 6 H) 242 4-OCF₃ 1,4 2,5- 1,4- α B 611 228-233 7.47(d, J= 9 Hz, 2 H), 7.42(d, J = 9 Hz, 2 H), 7.34(m, 4 H), 7.0(s, 1 H), 6.19phenyl piperazine- phenyl [M]⁺ (d, J = 1.8 Hz, 1 H), 4.5(m, 4 H),3.74(m, 1 H), 3.7-3.5(m, 10 H), 3.23(t, J = dione 9.5 Hz, 1 H), 1.35(d,J = 6.3 Hz, 3 H), 1.30(t, J = 7 Hz, 3 H) 243 4-OC₂F₅ 1,4 2,5- 1,4- α B661 8.20(d, J = 8.26 Hz, 2 H), 7.43(d, J = 8.30 Hz, 2 H), 7.36(d, J =8.26 Hz, phenyl piperazine- phenyl [M]⁺ 2 H), 7.22(d, J = 8.30 Hz, 2 H),6.89(s, 1 H), 6.20(d, J = 1.85 Hz, 1 H), 4.38 dione (s, 2 H), 4.18(s, 2H), 3.79-3.61(m, 4 H), 3.57(s, 3 H), 3.56(s, 3 H), 3.44(dd, J = 9.31,3.36 Hz, 1 H), 3.18(t, J = 9.48 Hz, 1 H), 1.36-1.23(m, 6 H) 244 4-OC₂F₅1,3 1,3,4- 1,4- α/β R 559 171-175 8.58(s, 1 H), 8.16(d, J = 8.7 Hz, 2H), 7.81(d, J = 8.7 Hz, 2 H), 7.52(d, J = phenyl triazole phenyl [M]⁺8.7 Hz, 2 H), 7.4(d, J = 8.7 Hz, 2 H), 6.93(s, 1 H), 6.3(d, J = 2 Hz)and 5.79 (dd, J = 10, 2 Hz, total of 1 H in a 1:3 α:β ratio), 3.51(m, 1H), 3.46(s, 3 H), 3.3(m, 1 H), 3.22(t, J = 9.3 Hz, 1 H), 2.58(s, 1 H),2.43(m, 1 H), 1.64(m, 1 H), 1.39(d, J = 6 Hz, 3 H) 245 4-OC₂F₅ 1,31,2,4- 1,4- β Q 572 151-155 8.52(s, 1 H), 8.16(d, J = 8.7 Hz, 2 H),7.81(d, J = 8.7 Hz, 2 H), 7.51(d, J = phenyl triazole phenyl [M]⁺ 8.4Hz, 2 H), 7.40(d, J = 8.7 Hz, 2 H), 6.94(s, 1 H), 5.73(dd, J = 10.2, 2Hz, 1 H), 3.7-3.3(series of m, 8 H), 2.81(t, J = 9 Hz, 1 H), 2.4(m, 1H), 1.6(m, 1 H), 1.37(d, J = 6.3 Hz, 3 H) 246 4-OCF₃ 1,3 1,2,4- 1,4- α P505 134-138 8.55(s, 1 H), 8.15(d, J = 7.9 Hz, 2 H), 7.79(d, J = 9.2 Hz,2 H), 7.54(d, J = phenyl triazole phenyl [M]⁺ 8.9 Hz, 2 H), 7.38(d, J =8.7 Hz, 2 H), 6.83(br s, 1 H), 6.13(d, J = 2.4 Hz, 1 H), 3.99-3.89(m, 1H), 2.35-2.24(m, 7 H), 2.05-1.98(m, 1 H), 1.91-1.68(m, 3 H), 1.28(d, J =6.0 Hz, 3 H) 247 4-OCF₃ 4,2 4,5-dihydro- 1,4- α B 568 8.02(d, J = 8.20Hz, 2 H), 7.52(d, J = 8.20 Hz, 2 H), 7.38(d, J = 8.24 Hz, phenyl oxazolephenyl [M⁺] 2 H), 7.22(d, J = 8.24 Hz, 2 H), 6.84(s, 1 H), 6.20(d, J =1.85 Hz, 1 H), 5.44(t, J = 9.42 Hz, 1 H), 4.82(t, J = 9.48 Hz, 1 H),4.28(t, J = 9.48 Hz, 1 H), 3.79- 3.61(m, 4 H), 3.57(s, 3 H), 3.56(s, 3H), 3.44(dd, J = 9.31, 3.36 Hz, 1 H), 3.18 (t, J = 9.48 Hz, 1 H),1.36-1.23(m, 6 H) 248 4-OCF₃ 3,6 pyridazine 1,4- α B 577 8.19(d, J = 8.9Hz, 2 H), 8.16(d, J = 8.9 Hz, 2 H), 7.94(s, 1 H), 7.90(s, 1 H), phenylphenyl [M]⁺ 7.61(d, J = 8.6 Hz, 2 H), 7.39(d, J = 8.6 Hz, 2 H), 6.91(s,1 H), 6.21(s, 1 H), 3.54-3.80(m, 5 H), 3.60(s, 3 H), 3.57(s, 3 H),3.21(t, J = 9.2 Hz, 1 H), 1.20- 1.35(m, 6 H) 249 4-CF₃ 4,2 1,3,4- 1,4- αB 566 8.15(d, J = 8.7 Hz, 2 H), 7.95(d, J = 8.7 Hz, 2 H), 7.75(d, J =8.7 Hz, 2 H), phenyl oxadiazolin- phenyl [M − H] 7.61(d, J = 8.7 Hz, 2H), 6.90(s, 1 H), 6.22(s, 1 H), 3.8-3.55(series of s and 5-one m, 11 H),3.21(t, J = 9.3 Hz, 1 H), 1.5(m, 6 H) ¹Het link: Atoms on Het to whichAr₃ and Ar₂ are attached respectively. ²Key to Sugars: See Table 4 ³AllNMR data measured in CDCl₃ at 300 or 400 MHz unless otherwise noted

TABLE 7

BAW 50 ug/cm2 BAW HTS Compound Ar1 Het Ar2 B A 1

B A 2

B A 3

B B 4

A B 5

A B 6

A B 7

A B 8

A B 9

A B 10

A B 11

A B 12

A B 13

B B 14

A B 15

B A 16

B A 17

B A 18

B B 19

B A 20

B A 21

B B 22

B B 23

B A 24

B B 25

A A 26

A A 27

A A 28

A B 29

A A 30

A A 31

A A 32

A A 33

A B 34

A B 35

A B 36

A B 37

A B 38

A B 39

A B 40

A B 41

A B 42

A B 43

A B 44

A B 45

A B 46

A B 47

A B 48

A B 49

A A 50

A B 51

A B 52

A A 53

A A 54

A A 55

A A 56

A A 57

A A 58

A A 59

A A 60

A A 61

A A 62

A A 63

A A 64

A A 65

A A 66

A B 67

A B 68

B B 69

B A 70

B A 71

A A 72

A B 73

A B 74

B A 75

B B 76

B B 77

A B 78

A B 79

A A 80

A A 81

A B 82

A B 83

A B 84

A B 85

A B 86

A B 87

A B 88

A B 89

A B 90

A B 91

A B 92

A A 93

A B 94

A B 95

A B 96

A B 97

A B 98

A B 99

A B 100

A B 101

B B 102

A B 103

A B 104

A B 105

A B 106

A A 107

A B 108

A A 109

A B 110

A A 111

A B 112

A B 113

A A 114

A B 115

A B 116

B B 117

A B 118

A A 119

A A 120

A B 121

A A 122

A B 123

A B 124

A B 125

A B 126

A B 127

A B 128

A B 129

A A 130

B B 131

A B 132

A B 133

A B 134

A B 135

A B 136

A B 137

A A 138

A A 139

A B 140

A A 141

A A 142

A B 143

A B 144

A B 145

A B 146

B B 147

A B 148

A B 149

B B 150

A B 151

A B 152

A B 153

A B 154

A B 155

A B 156

B A 157

A A 158

A A 159

A A 160

A A 161

A B 162

B B 163

B B 164

A B 165

A B 166

A B 167

A A 168

A B 169

A B 170

A A 171

A B 172

A A 173

A A 174

A A 175

A B 176

B A 177

A B 178

A B 179

A B 180

A A 181

B B 182

A A 183

B B 184

B B 185

A B 186

A A 187

A B 188

A A 189

A A 190

A A 191

A A 192

A B 193

A A 194

A B 195

A A 196

A A 197

A A 198

A A 199

A A 200

A A 201

A A 202

A A 203

A A 204

A A 205

A A 206

A B 207

A A 208

A A 209

A A 210

A A 211

A A 212

B B 213

A A 214

A A 215

A A 216

A A 217

A B 218

A B 219

A B 220

A B 221

A B 222

A B 223

A B 224

A B 225

B B 226

B B 227

B B 228

A A 229

A B 230

B A 231

A A 232

A B 233

B B 234

B A 235

A B 236

A B 237

A B 238

B B 239

A A 240

B B 241

A B 242

B B 243

A B 244

A B 245

A B 246

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B B 248

B B 249

A B 250

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A A 253

A A 254

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A A 256

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A A 258

A B 259

BAW 50 ug/ cm2 BAW HTS Compound J L K Q R1 R2 R3 R4 anomer sugar B A 1CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose B A 2 CH double N O OCH₃OCH₃ OCH₃ CH₃ α L-rhamnose B A 3 CH double N O OCH₃ OCH₃ OCH₃ CH₃ αL-rhamnose B B 4 CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 5 CHdouble N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 6 CH double N O OCH₃ OCH₃OCH₃ CH₃ α L-rhamnose A B 7 CH double N O OCH₃ OCH₃ OCH₃ CH₃ αL-rhamnose A B 8 CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 9 CHdouble N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 10 CH double N O OCH₃OCH₃ OCH₃ CH₃ α L-rhamnose A B 11 CH double N O OCH₃ OCH₃ OCH₃ CH₃ αL-rhamnose A B 12 CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 13CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose B B 14 CH double N O OCH₃OCH₃ OCH₃ CH₃ α L-rhamnose A B 15 CH double N O OCH₃ OCH₃ OCH₃ CH₃ αL-rhamnose B A 16 CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose B A 17CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose B A 18 CH double N O OCH₃OCH₃ OCH₃ CH₃ α L-rhamnose B B 19 CH double N O OCH₃ OCH₃ OCH₃ CH₃ αL-rhamnose B A 20 CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose B A 21CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose B B 22 CH double N O OCH₃OCH₃ OCH₃ CH₃ α L-rhamnose B B 23 CH double N O OCH₃ OCH₃ OCH₃ CH₃ αL-rhamnose B A 24 CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose B B 25CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A A 26 CH double N O OCH₃OCH₃ OCH₃ CH₃ α L-rhamnose A A 27 CH double N O OCH₃ OCH₃ OCH₃ CH₃ αL-rhamnose A A 28 CH double N O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A B 29CH double N O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A A 30 CH double N O OCH₃OCH₃ OCH₃ CH₃ α L-rhamnose A A 31 CH double N O OC₂H₅ OC₂H₅ OC₂H₅ CH₃ αL-rhamnose A A 32 CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A A 33CH double N O OC₂H₅ OC₂H₅ OC₂H₅ CH₃ α L-rhamnose A B 34 CH double N OOCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 35 CH double N O OCH₃ OCH₃ OCH₃ CH₃α L-rhamnose A B 36 CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 37CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 38 CH double N O OCH₃OCH₃ OCH₃ CH₃ α L-rhamnose A B 39 CH double N O OCH₃ OCH₃ OCH₃ CH₃ αL-rhamnose A B 40 CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 41CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 42 CH double N O OCH₃OCH₃ OCH₃ CH₃ α L-rhamnose A B 43 CH double N O OCH₃ OCH₃ OCH₃ CH₃ αL-rhamnose A B 44 CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 45CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 46 CH double N O OCH₃OCH₃ OCH₃ CH₃ α L-rhamnose A B 47 CH double N O OCH₃ OCH₃ OCH₃ CH₃ αL-rhamnose A B 48 CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 49CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A A 50 CH double N O OCH₃OCH₃ OCH₃ CH₃ α L-rhamnose A B 51 CH double N O OCH₃ OCH₃ OCH₃ CH₃ αL-rhamnose A B 52 CH double N O OC₂H₅ OC₂H₅ OC₂H₅ CH₃ α L-rhamnose A A53 CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A A 54 CH double N OOCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A A 55 CH double N O OCH₃ OCH₃ OCH₃ CH₃α L-rhamnose A A 56 CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A A 57CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A A 58 CH double N O OCH₃OCH₃ OCH₃ CH₃ α L-rhamnose A A 59 CH double N O OCH₃ OCH₃ OCH₃ CH₃ αL-rhamnose A A 60 CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A A 61CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A A 62 CH double N O OCH₃OCH₃ OCH₃ CH₃ α L-rhamnose A A 63 CH double N O OCH₃ OCH₃ OCH₃ CH₃ αL-rhamnose A A 64 CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A A 65CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A A 66 OH double N O OCH₃OCH₃ OCH₃ CH₃ α L-rhamnose A B 67 CH double N O OCH₃ OCH₃ OCH₃ CH₃ αL-rhamnose A B 68 CH double N O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose B B 69CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose B A 70 CH double N O OCH₃OCH₃ OCH₃ CH₃ α L-rhamnose B A 71 CH double N O OCH₃ OCH₃ OCH₃ CH₃ αL-rhamnose A A 72 CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 73CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 74 CH double N O OCH₃OC₃H₇ OCH₃ CH₃ α L-rhamnose B A 75 CH double N O OCH₃ OCH₃ OCH₃ CH₃ αL-rhamnose B B 76 CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose B B 77CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 78 CH double N O OCH₃OCH₃ OCH₃ CH₃ α L-rhamnose A B 79 CH double N O OCH₃ OCH₃ OCH₃ CH₃ αL-rhamnose A A 80 CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A A 81CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 82 CH double N O OCH₃OCH₃ OCH₃ CH₃ α L-rhamnose A B 83 CH double N O OCH₃ OCH₃ OCH₃ CH₃ αL-rhamnose A B 84 CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 85CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 86 CH double N O OCH₃OCH₃ OCH₃ CH₃ α L-rhamnose A B 87 CH double N O OCH₃ OCH₃ OCH₃ CH₃ αL-rhamnose A B 88 CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 89CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 90 CH double N O OCH₃OCH₃ OCH₃ CH₃ α L-rhamnose A B 91 CH double N O OCH₃ OCH₃ OCH₃ CH₃ αL-rhamnose A B 92 CH double N O OC₂H₅ OC₂H₅ OC₂H₅ CH₃ α L-rhamnose A A93 CH double N O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A B 94 CH double N OOCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 95 CH double N O OCH₃ OCH₃ OCH₃ CH₃α L-rhamnose A B 96 CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 97CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 98 CH double N O OCH₃OCH₃ OCH₃ CH₃ α L-rhamnose A B 99 CH double N O OCH₃ OCH₃ OCH₃ CH₃ αL-rhamnose A B 100 CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 101CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose B B 102 CH double N O OCH₃OCH₃ OCH₃ CH₃ α L-rhamnose A B 103 CH double N O OCH₃ OCH₃ OCH₃ CH₃ αL-rhamnose A B 104 CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 105CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 106 CH double N O OCH₃OC₃H₇ OCH₃ CH₃ α L-rhamnose A A 107 CH double N O OCH₃ OC₃H₇ OCH₃ CH₃ αL-rhamnose A B 108 CH double N O OCH₃ OC₃H₇ OCH₃ CH₃ α L-rhamnose A A109 CH double N O OCH₃ OC₄H₉ OCH₃ CH₃ α L-rhamnose A B 110 CH double N OOCH₃ OC₃H₇ OCH₃ CH₃ α L-rhamnose A A 111 CH double N O OCH₃ OCH₃ CH CH₃α L-rhamnose A B 112 CH double N O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A B113 CH double N O OCH₃ OCH₃ OC₃H₇ CH₃ α L-rhamnose A A 114 CH double N OOCH₃ OCH₃ OCH₃ CH₂OCH₃ α D-glucose A B 115 CH double N O OCH₃ OC₂H₅ OCH₃CH₃ α L-rhamnose A B 116 CH double N O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnoseB B 117 CH double N O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A B 118 CH doubleN O OCH₃ OC₃H₇ OCH₃ CH₃ α L-rhamnose A A 119 CH double N O OCH₃ OCH₃OCH₃ CH₂OCH₃ α L-mannose A A 120 CH double N O OCH₃ OC₂H₅ OCH₃ CH₃ αL-rhamnose A B 121 CH double N O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A A122 CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-fucose A B 123 CH double N OOCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A B 124 CH double N O OCH₃ OC₂H₅ OCH₃CH₃ α L-rhamnose A B 125 CH double N O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnoseA B 126 CH double N O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A B 127 CH doubleN O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A B 128 CH double N O OCH₃ OC₂H₅OCH₃ CH₃ α L-rhamnose A B 129 CH double N O OCH₃ OC₂H₅ OCH₃ CH₃ αL-rhamnose A A 130 CH double N O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose B B131 CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 132 CH double N OOCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 133 CH double N O OCH₃ OCH₃ OCH₃ CH₃α L-rhamnose A B 134 CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B135 CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 136 CH double N OOCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 137 CH double N O OCH₃ OCH₃ OCH₃ CH₃α L-rhamnose A A 138 CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A A139 CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 140 CH double N OOCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A A 141 CH double N O OCH₃ OCH₃ OCH₃ CH₃α L-rhamnose A A 142 CH double N O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A B143 CH double N O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A B 144 CH double N OOCH₃ OC₃H₇ OCH₃ CH₃ α L-rhamnose A B 145 CH double N O OCH₃ OC₄H₉ OCH₃CH₃ α L-rhamnose A B 146 CH double N O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnoseB B 147 CH double N O OCH₃ OC₂H₅ OCH₂ CH₃ α L-rhamnose A B 148 CH doubleN O CCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A B 149 CH double N O OCH₃ OC₂H₅OCH₃ CH₃ α L-rhamnose B B 150 CH double N O OCH₃ OC₂H₅ OCH₃ CH₃ αL-rhamnose A B 151 CH double N O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A B152 CH double N O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A B 153 CH double N OOCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A B 154 CH double N O OCH₃ OC₂H₅ OCH₃CH₃ α L-rhamnose A B 155 CH double N O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnoseA B 156 CH double N O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose B A 157 CH doubleN O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A A 158 CH double N O OCH₃ OCH₃ OCH₃CH₃ α L-rhamnose A A 159 CH double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose AA 160 CH double N O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A A 161 CH double NO OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A B 162 CH double N O OCH₃ OC₃H₇ OCH₃CH₃ α L-rhamnose B B 163 CH double N O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnoseB B 164 C—CH₃ double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 165 C—CH₃double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 166 C—CH₃ double N O OCH₃OCH₃ OCH₃ CH₃ α L-rhamnose A B 167 C—CH₃ double N O OCH₃ OCH₃ OCH₃ CH₃ αL-rhamnose A A 168 C—CH₃ double N O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B169 C—CF₃ double N O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A B 170 N/A singleN O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A A 171 C═O single NH O OCH₃ OCH₃OCH₃ CH₃ α L-rhamnose A B 172 NH single C═O O OCH₃ OCH₃ OCH₃ CH₃ αL-rhamnose A A 173 NH single C═O O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A A174 NH single C═O O OCH₃ OCH₃ OCH₃ CH₃ β L-rhamnose A A 175 NH singleC═O O OCH₃ OC₄H₉ OCH₃ CH₃ α L-rhamnose A B 176 NH single C═S O OCH₃ OCH₃OCH₃ CH₃ α L-rhamnose B A 177 NH single C═O S OCH₃ OC₂H₅ OCH₃ CH₃ αL-rhamnose A B 178 NH single C═O O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A B179 NH single C═O O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A B 180 NH singleC═O O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A A 181 NH single C═O O OCH₃OC₂H₅ OCH₃ CH₃ α L-rhamnose B B 182 NH single C═O O OCH₃ OC₂H₅ OCH₃ CH₃β L-rhamnose A A 183 NH single C═O O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose BB 184 NH single C═O O OCH₃ OC₂H₅ OCH₃ CH₃ β L-rhamnose B B 185 NH singleC═O O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A B 186 NH single C═O O OCH₃OC₂H₅ OCH₃ CH₃ α L-rhamnose A A 187 NH single C═O O OCH₃ OC₂H₅ OCH₃ CH₃α L-rhamnose A B 188 NH single C═O O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose AA 189 NH single C═O O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A A 190 NH singleC═O O OCH₃ OCH₃ OCH₃ CH₃ β L-rhamnose A A 191 NH single C═O O OCH₃ OCH₃OCH₃ CH₃ α L-rhamnose A A 192 NH single C═O O OCH₃ OC₂H₅ OCH₃ CH₃ αL-rhamnose A B 193 NH single C═O O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A A194 NH single C═O O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 195 NH singleC═O O OCH₃ OCH₃ OCH₃ CH₃ β L-rhamnose A A 196 NH single C═O O OCH₃ OCH₃OCH₃ CH₃ α L-rhamnose A A 197 NH single C═O O OCH₃ OC₄H₉ OCH₃ CH₃ αL-rhamnose A A 198 NH single C═O O OCH₃ OC₄H₉ OCH₃ CH₃ α L-rhamnose A A199 NH single C═O O OCH₃ OC₄H₉ OCH₃ CH₃ β L-rhamnose A A 200 NH singleC═O O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A A 201 NH single C═O O OCH₃ OC₂H₅OCH₃ CH₃ α L-rhamnose A A 202 NH single C═O O OCH₃ OC₂H₅ OCH₃ CH₃ βL-rhamnose A A 203 NH single C═S O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A A204 NH single C═O O OCH₃ OCH₂CH═CH₂ OCH₃ CH₃ α L-rhamnose A A 205 NHsingle C═O O OCH₃ OCH₂CH═CH₂ OCH₃ CH₃ α L-rhamnose A A 206 NH single C═OO OC₂H₅ OC₂H₅ OC₂H₅ CH₃ α L-rhamnose A B 207 NH single C═O O OCH₃ OC₃H₇OCH₃ CH₃ α L-rhamnose A A 208 NH single C═O O OCH₃ OCH₃ OCH₃ CH₃ βL-rhamnose A A 209 NH single C═O O OCH₃ OC₃H₇ OCH₃ CH₃ α L-rhamnose A A210 NH single C═O O OCH₃ OC₂H₅ OCH₃ CH₃ β L-rhamnose A A 211 NH singleC═O S OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A A 212 NH single C═O O OCH₃ OCH₃OCH₃ H α/β L-xylose B B 213 NH single C═O O OCH₃ OCH₃ OCH₃ H α/βL-xylose A A 214 NH single C═O O OCH₃ OCH₃ OCH₃ H α L-lyxose A A 215 NHsingle C═O O OCH₃ OCH₃ OCH₃ H β L-lyxose A A 216 NH single C═O O OCH₃OC₃H₇ OCH₃ CH₃ α L-rhamnose A A 217 NH single C═O O OCH₃ OCH₃ OCH₃ OCH₃α L-glucose A B 218 NH single C═O O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A B219 NH single C═O O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A B 220 NH singleC═O O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A B 221 NH single C═O O OCH₃OC₂H₅ OCH₃ CH₃ α L-rhamnose A B 222 NH single C═O O OCH₃ OC₂H₅ OCH₃ CH₃α L-rhamnose A B 223 NH single C═O O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose AB 224 NH single C═O O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A B 225 NH singleC═O O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose B B 226 NH single C═O O OCH₃OC₂H₅ OCH₃ CH₃ α L-rhamnose B B 227 NH single C═O O OCH₃ OC₂H₅ OCH₃ CH₃β L-rhamnose B B 228 NH single C═O O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose AA 229 NH single C═O O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose A B 230 NH singleC═O O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose B A 231 NH single C═O O OCH₃ OCH₃OCH₃ CH₃ α L-rhamnose A A 232 NH single C═O O OCH₃ OCH₃ OCH₃ CH₃ αL-rhamnose A B 233 NH single C═O O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose B B234 NH single C═O O OCH₃ OCH₃ OCH₃ CH₃ α L-rhamnose B A 235 NH singleC═O O OCH₃ OCH₃ OCH₃ CH₃ α L-thamnose A B 236 NH single C═O O CCH₃ OC₃H₇OCH₃ CH₃ α L-rhamnose A B 237 NH single C═O O OCH₃ OC₂H₅ OCH₃ CH₃ αL-rhamnose A B 238 NH single C═O O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose B B239 NH single C═O O CCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A A 240 NH singleC═O O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose B B 241 NH single C═O O OCH₃OC₂H₅ OCH₃ CH₃ α L-rhamnose A B 242 NH single C═O O OCH₃ OC₂H₅ OCH₃ CH₃α L-rhamnose B B 243 NH single C═O O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose AB 244 NH single C═O O H OCH₃ CH CH₃ α/β L- oleandrose A B 245 NH singleC═O O H OCH₃ OCH₃ CH₃ β L-oleandrose A B 246 NH single C═O O H H N(Me)2CH₃ α D- forosamine A B 247 NH single C═O O OCH₃ OC₂H₅ OCH₃ CH₃ αL-rhamnose B B 248 NH single C═O O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose B B249 NH single C═O O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A B 250 NCH₃ singleC═O O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A B 251 NCH₃ single C═O O OCH₃OC₂H₅ OCH₃ CH₃ α L-rhamnose A B 252 NCH₃ single C═O O OCH₃ OC₂H₅ OCH₃CH₃ α L-rhamnose A A 253 NCH₂CH₃ single C═O O OCH₃ OC₃H₇ OCH₃ CH₃ αL-rhamnose A A 254 NCH₂OCH₃ single C═O O OCH₃ OC₂H₅ OCH₃ CH₃ αL-rhamnose A B 255 NCH₂OCH₃ single C═O O OCH₃ OC₂H₅ OCH₃ CH₃ αL-rhamnose A A 256 NCH₂CH═CH₂ single C═O O OCH₃ OC₂H₅ OCH₃ CH₃ αL-rhamnose A B 257 NCH₂OH single C═O O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnoseA A 258 NCOCH₃ single C═O O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose A B 259NCOCH₂CH₂— CO₂CH₃ single C═O O OCH₃ OC₂H₅ OCH₃ CH₃ α L-rhamnose

Acid & Salt Derivatives, and Solvates

The compounds disclosed in this invention can be in the form ofpesticidally acceptable acid addition salts.

By way of non-limiting example, an amine function can form salts withhydrochloric, hydrobromic, sulfuric, phosphoric, acetic, benzoic,citric, malonic, salicylic, malic, fumaric, oxalic, succinic, tartaric,lactic, gluconic, ascorbic, maleic, aspartic, benzenesulfonic,methanesulfonic, ethanesulfonic, hydroxymethanesulfonic, andhydroxyethanesulfonic, acids.

Additionally, by way of non-limiting example, an acid function can formsalts including those derived from alkali or alkaline earth metals andthose derived from ammonia and amines. Examples of preferred cationsinclude sodium, potassium, magnesium, and aminium cations.

The salts are prepared by contacting the free base form with asufficient amount of the desired acid to produce a salt. The free baseforms may be regenerated by treating the salt with a suitable diluteaqueous base solution such as dilute aqueous NaOH, potassium carbonate,ammonia, and sodium bicarbonate.

As an example, in many cases, a pesticide is modified to a more watersoluble form e.g. 2,4-dichlorophenoxy acetic acid dimethyl amine salt isa more water soluble form of 2,4-dichlorophenoxy acetic acid, a wellknown herbicide.

The compounds disclosed in this invention can also form stable complexeswith solvent molecules that remain intact after the non-complexedsolvent molecules are removed from the compounds. These complexes areoften referred to as “solvates”.

Stereoisomers

Certain compounds disclosed in this invention can exist as one or morestereoisomers. The various stereoisomers include geometric isomers,diastereomers, and enantiomers. Thus, the compounds disclosed in thisinvention include racemic mixtures, individual stereoisomers, andoptically active mixtures.

It will be appreciated by those skilled in the art that one stereoisomermay be more active than the others. Individual stereoisomers andoptically active mixtures may be obtained by selective syntheticprocedures, by conventional synthetic procedures using resolved startingmaterials, or by conventional resolution procedures.

Pests

In another embodiment, the invention disclosed in this document can beused to control pests.

In another embodiment, the invention disclosed in this document can beused to control pests of the Phylum Nematoda.

In another embodiment, the invention disclosed in this document can beused to control pests of the Phylum Arthropoda.

In another embodiment, the invention disclosed in this document can beused to control pests of the Subphylum Chelicerata.

In another embodiment, the invention disclosed in this document can beused to control pests of the Class Arachnida.

In another embodiment, the invention disclosed in this document can beused to control pests of the Subphylum Myriapoda.

In another embodiment, the invention disclosed in this document can beused to control pests of the Class Symphyla.

In another embodiment, the invention disclosed in this document can beused to control pests of the Subphylum Hexapoda.

In another embodiment, the invention disclosed in this document can beused to control pests of the Class Insecta.

In another embodiment, the invention disclosed in this document can beused to control Coleoptera (beetles). A non-exhaustive list of thesepests includes, but is not limited to, Acanthoscelides spp. (weevils),Acanthoscelides obtectus (common bean weevil), Agrilus planipennis(emerald ash borer), Agriotes spp. (wireworms), Anoplophora glabripennis(Asian longhomed beetle), Anthonomus spp. (weevils), Anthonomus grandis(boll weevil), Aphidius spp., Apion spp. (weevils), Apogonia spp.(grubs), Ataenius spretulus (Black Turgrass Ataenius), Atomaria linearis(pygmy mangold beetle), Aulacophore spp., Bothynoderes punctiventris(beet root weevil), Bruchus spp. (weevils), Bruchus pisorum (peaweevil), Cacoesia spp., Callosobruchus maculatus (southern cow peaweevil), Carpophilus hemipteras (dried fruit beetle), Cassida vittata,Cerosterna spp, Cerotoma spp. (chrysomeids), Cerotoma trifurcata (beanleaf beetle), Ceutorhynchus spp. (weevils), Ceutorhynchus assimilis(cabbage seedpod weevil), Ceutorhynchus napi (cabbage curculio),Chaetocnema spp. (chrysomelids), Colaspis spp. (soil beetles), Conoderusscalaris, Conoderus stigmosus, Conotrachelus nenuphar (plum curculio),Cotinus nitidis (Green June beetle), Crioceris asparagi (asparagusbeetle), Cryptolestes ferrugineus (rusty grain beetle), Cryptolestespusillus (flat grain beetle), Cryptolestes turcicus (Turkish grainbeetle), Ctenicera spp. (wireworms), Curculio spp. (weevils),Cyclocephala spp. (grubs), Cylindrocpturus adspersus (sunflower stemweevil), Deporaus marginatus (mango leaf-cutting weevil), Dermesteslardarius (larder beetle), Dermestes maculates (hide beetle), Diabroticaspp. (chrysolemids), Epilachna varivestis (Mexican bean beetle),Faustinus cubae, Hylobius pales (pales weevil), Hypera spp. (weevils),Hypera postica (alfalfa weevil), Hyperdoes spp. (Hyperodes weevil),Hypothenemus hampei (coffee berry beetle), Ips spp. (engravers),Lasioderma serricorne (cigarette beetle), Leptinotarsa decemlineata(Colorado potato beetle), Liogenys fuscus, Liogenys suturalis,Lissorhoptrus oryzophilus (rice water weevil), Lyctus spp. (woodbeetles/powder post beetles), Maecolaspis joliveti, Megascelis spp.,Melanotus communis, Meligethes spp., Meligethes aeneus (blossom beetle),Melolontha melolontha (common European cockchafer), Oberea brevis,Oberea linearis, Oryctes rhinoceros (date palm beetle), Oryzaephilusmercator (merchant grain beetle), Oryzaephilus surinamensis (sawtoothedgrain beetle), Otiorhynchus spp. (weevils), Oulema melanopus (cerealleaf beetle), Oulema oryzae, Pantomorus spp. (weevils), Phyllophaga spp.(May/June beetle), Phyllophaga cuyabana, Phyllotreta spp.(chrysomelids), Phynchites spp., Popillia japonica (Japanese beetle),Prostephanus truncates (larger grain borer), Rhizopertha dominica(lesser grain borer), Rhizotrogus spp. (Eurpoean chafer), Rhynchophorusspp. (weevils), Scolytus spp. (wood beetles), Shenophorus spp.(Billbug), Sitona lineatus (pea leaf weevil), Sitophilus spp. (grainweevils), Sitophilus granaries (granary weevil), Sitophilus oryzae (riceweevil), Stegobium paniceum (drugstore beetle), Tribolium spp. (flourbeetles), Tribolium castaneum (red flour beetle), Tribolium confusum(confused flour beetle), Trogoderma variabile (warehouse beetle), andZabrus tenebioides.

In another embodiment, the invention disclosed in this document can beused to control Dermaptera (earwigs).

In another embodiment, the invention disclosed in this document can beused to control Dictyoptera (cockroaches). A non-exhaustive list ofthese pests includes, but is not limited to, Blattella germanica (Germancockroach), Blatta orientalis (oriental cockroach), Parcoblattapennylvanica, Periplaneta americana (American cockroach), Periplanetaaustraloasiae (Australian cockroach), Periplaneta brunnea (browncockroach), Periplaneta fuliginosa (smokybrown cockroach), Pyncoselussuninamensis (Surinam cockroach), and Supella longipalpa (brownbandedcockroach).

In another embodiment, the invention disclosed in this document can beused to control Diptera (true flies). A non-exhaustive list of thesepests includes, but is not limited to, Aedes spp. (mosquitoes), Agromyzafrontella (alfalfa blotch leafminer), Agromyza spp. (leaf miner flies),Anastrepha spp. (fruit flies), Anastrepha suspensa (Caribbean fruitfly), Anopheles spp. (mosquitoes), Batrocera spp. (fruit flies),Bactrocera cucurbitae (melon fly), Bactrocera dorsalis (oriental fruitfly), Ceratitis spp. (fruit flies), Ceratitis capitata (Mediterraneafruit fly), Chrysops spp. (deer flies), Cochliomyia spp. (screwworms),Contarinia spp. (Gall midges), Culex spp. (mosquitoes), Dasineura spp.(gall midges), Dasineura brassicae (cabbage gall midge), Delia spp.,Delia platura (seedcorn maggot), Drosophila spp. (vinegar flies), Fanniaspp. (filth flies), Fannia canicularis (little house fly), Fanniascalaris (latrine fly), Gasterophilus intestinalis (horse bot fly),Gracillia perseae, Haematobia irritans (horn fly), Hylemyia spp. (rootmaggots), Hypoderma lineatum (common cattle grub), Liriomyza spp.(leafminer flies), Liriomyza brassica (serpentine leafminer), Melophagusovinus (sheep ked), Musca spp. (muscid flies), Musca autumnalis (facefly), Musca domestica (house fly), Oestrus ovis (sheep bot fly),Oscinella frit (frit fly), Pegomyia betae (beet leafminer), Phorbiaspp., Psila rosae (carrot rust fly), Rhagoletis cerasi (cherry fruitfly), Rhagoletis pomonella (apple maggot), Sitodiplosis mosellana(orange wheat blossom midge), Stomoxys calcitrans (stable fly), Tabanusspp. (horse flies), and Tipula spp. (crane flies).

In another embodiment, the invention disclosed in this document can beused to control Hemiptera (true bugs). A non-exhaustive list of thesepests includes, but is not limited to, Acrosternum hilare (green stinkbug), Blissus leucopterus (chinch bug), Calocoris norvegicus (potatomirid), Cimex hemipterus (tropical bed bug), Cimex lectularius (bedbug), Dagbertus fasciatus, Dichelops furcatus, Dysdercus suturellus(cotton stainer), Edessa meditabunda, Eurygaster maura (cereal bug),Euschistus heros, Euschistus servus (brown stink bug), Helopeltisantonii, Helopeltis theivora (tea blight plantbug), Lagynotomus spp.(stink bugs), Leptocorisa oratorius, Leptocorisa varicornis, Lygus spp.(plant bugs), Lygus hesperus (western tarnished plant bug),Maconellicoccus hirsutus, Neurocolpus longirostris, Nezara viridula(southern green stink bug), Phytocoris spp. (plant bugs), Phytocoriscalifornicus, Phytocoris relativus, Piezodorus guildingi, Poecilocapsuslineatus (fourlined plant bug), Psallus vaccinicola, Pseudacystaperseae, Scaptocoris castanea, and Triatoma spp. (bloodsucking conenosebugs/kissing bugs).

In another embodiment, the invention disclosed in this document can beused to control Homoptera (aphids, scales, whiteflies, leafhoppers). Anon-exhaustive list of these pests includes, but is not limited to,Acrythosiphon pisum (pea aphid), Adelges spp. (adelgids), Aleurodesproletella (cabbage whitefly), Aleurodicus disperses, Aleurothrixusfloccosus (woolly whitefly), Aluacaspis spp., Amrasca bigutellabigutella, Aphrophora spp. (leafhoppers), Aonidiella aurantii(California red scale), Aphis spp. (aphids), Aphis gossypii (cottonaphid), Aphis pomi (apple aphid), Aulacorthum solani (foxglove aphid),Bemisia spp. (whiteflies), Bemisia argentifolii, Bemisia tabaci(sweetpotato whitefly), Brachycolus noxius (Russian aphid),Brachycorynella asparagi (asparagus aphid), Brevennia rehi, Brevicorynebrassicae (cabbage aphid), Ceroplastes spp. (scales), Ceroplastes rubens(red wax scale), Chionaspis spp. (scales), Chrysomphalus spp. (scales),Coccus spp. (scales), Dysaphis plantaginea (rosy apple aphid), Empoascaspp. (leafhoppers), Eriosoma lanigerum (woolly apple aphid), Iceryapurchasi (cottony cushion scale), Idioscopus nitidulus (mangoleafhopper), Laodelphax striatellus (smaller brown planthopper),Lepidosaphes spp., Macrosiphum spp., Macrosiphum euphorbiae (potatoaphid), Macrosiphum granarium (English grain aphid), Macrosiphum rosae(rose aphid), Macrosteles quadrilineatus (aster leafhopper), Mahanarvafrimbiolata, Metopolophium dirhodum (rose grain aphid), Mictislongicornis, Myzus persicae (green peach aphid), Nephotettix spp.(leafhoppers), Nephotettix cinctipes (green leafhopper), Nilaparvatalugens (brown planthopper), Parlatoria pergandii (chaff scale),Parlatoria ziziphi (ebony scale), Peregrinus maidis (corn delphacid),Philaenus spp. (spittlebugs), Phylloxera vitifoliae (grape phylloxera),Physokermes piceae (spruce bud scale), Planococcus spp. (mealybugs),Pseudococcus spp. (mealybugs), Pseudococcus brevipes (pine applemealybug), Quadraspidiotus perniciosus (San Jose scale), Rhapalosiphumspp. (aphids), Rhapalosiphum maida (corn leaf aphid), Rhapalosiphum padi(oat bird-cherry aphid), Saissetia spp. (scales), Saissetia oleae (blackscale), Schizaphis graminum (greenbug), Sitobion avenae (English grainaphid), Sogatella furcifera (white-backed planthopper), Therioaphis spp.(aphids), Toumeyella spp. (scales), Toxoptera spp. (aphids),Trialeurodes spp. (whiteflies), Trialeurodes vaporariorum (greenhousewhitefly), Trialeurodes abutiloneus (bandedwing whitefly), Unaspis spp.(scales), Unaspis yanonensis (arrowhead scale), and Zulia entreriana.

In another embodiment, the invention disclosed in this document can beused to control Hymenoptera (ants, wasps, and bees). A non-exhaustivelist of these pests includes, but is not limited to, Acromyrrmex spp.,Athalia rosae, Atta spp. (leafcutting ants), Camponotus spp. (carpenterants), Diprion spp. (sawflies), Formica spp. (ants), Iridomyrmex humilis(Argentine ant), Monomorium ssp., Monomorium minumum (little black ant),Monomorium pharaonis (Pharaoh ant), Neodiprion spp. (sawflies),Pogonomyrmex spp. (harvester ants), Polistes spp. (paper wasps),Solenopsis spp. (fire ants), Tapoinoma sessile (odorous house ant),Tetranomorium spp. (pavement ants), Vespula spp. (yellow jackets), andXylocopa spp. (carpenter bees).

In another embodiment, the invention disclosed in this document can beused to control Isoptera (termites). A non-exhaustive list of thesepests includes, but is not limited to, Coptotermes spp., Coptotermescurvignathus, Coptotermes frenchii, Coptotermes formosanus (Formosansubterranean termite), Cornitermes spp. (nasute termites), Cryptotermesspp. (drywood termites), Heterotermes spp. (desert subterraneantermites), Heterotermes aureus, Kalotermes spp. (drywood termites),Incistitermes spp. (drywood termites), Macrotermes spp. (fungus growingtermites), Marginitermes spp. (drywood termites), Microcerotermes spp.(harvester termites), Microtermes obesi, Procornitermes spp.,Reticulitermes spp. (subterranean termites), Reticulitermes banyulensis,Reticulitermes grassei, Reticulitermes flavipes (eastern subterraneantermite), Reticulitermes hageni, Reticulitermes hesperus (westernsubterranean termite), Reticulitermes santonensis, Reticulitermessperatus, Reticulitermes tibialis, Reticulitermes virginicus,Schedorhinotermes spp., and Zootermopsis spp. (rotten-wood termites).

In another embodiment, the invention disclosed in this document can beused to control Lepidoptera (moths and butterflies). A non-exhaustivelist of these pests includes, but is not limited to, Achoea janata,Adoxophyes spp., Adoxophyes orana, Agrotis spp. (cutworms), Agrotisipsilon (black cutworm), Alabama argillacea (cotton leafworm), Amorbiacuneana, Amyelosis transitella (navel orangeworm), Anacamptodesdefectaria, Anarsia lineatella (peach twig borer), Anomis sabulifera(jute looper), Anticarsia gemmatalis (velvetbean caterpillar), Archipsargyrospila (fruittree leafroller), Archips rosana (rose leaf roller),Argyrotaenia spp. (tortricid moths), Argyrotaenia citrana (orangetortrix), Autographa gamma, Bonagota cranaodes, Borbo cinnara (rice leaffolder), Bucculatrix thurberiella (cotton leafperforator), Caloptiliaspp. (leaf miners), Capua reticulana, Carposina niponensis (peach fruitmoth), Chilo spp., Chlumetia transversa (mango shoot borer),Choristoneura rosaceana (obliquebanded leafroller), Chrysodeixis spp.,Cnaphalocerus medinalis (grass leafroller), Colias spp., Conpomorphacramerella, Cossus cossus (carpenter moth), Crambus spp. (Sod webworms),Cydia funebrana (plum fruit moth), Cydia molesta (oriental fruit moth),Cydia nignicana (pea moth), Cydia pomonella (codling moth), Darnadiducta, Diaphania spp. (stem borers), Diatraea spp. (stalk borers),Diatraea saccharalis (sugarcane borer), Diatraea graniosella(southwester corn borer), Earias spp. (bollworms), Earias insulata(Egyptian bollworm), Earias vitella (rough northern bollworm),Ecdytopopha aurantianum, Elasmopalpus lignosellus (lesser cornstalkborer), Epiphysias postruttana (light brown apple moth), Ephestia spp.(flour moths), Ephestia cautella (almond moth), Ephestia elutella(tobbaco moth), Ephestia kuehniella (Mediterranean flour moth), Epimecesspp., Epinotia aporema, Erionota thrax (banana skipper), Eupoeciliaambiguella (grape berry moth), Euxoa auxiliaris (army cutworm), Feltiaspp. (cutworms), Gortyna spp. (stemborers), Grapholita molesta (orientalfruit moth), Hedylepta indicata (bean leaf webber), Helicoverpa spp.(noctuid moths), Helicoverpa armigera (cotton bollworm), Helicoverpa zea(bollworm/corn earworm), Heliothis spp. (noctuid moths), Heliothisvirescens (tobacco budworm), Hellula undalis (cabbage webworm),Indarbela spp. (root borers), Keiferia lycopersicella (tomato pinworm),Leucinodes orbonalis (eggplant fruit borer), Leucoptera malifoliella,Lithocollectis spp., Lobesia botrana (grape fruit moth), Loxagrotis spp.(noctuid moths), Loxagrotis albicosta (western bean cutworm), Lymantriadispar (gypsy moth), Lyonetia clerkella (apple leaf miner), Mahasenacorbetti (oil palm bagworm), Malacosoma spp. (tent caterpillars),Mamestra brassicae (cabbage armyworm), Maruca testulalis (bean podborer), Metisa plana (bagworm), Mythimna unipuncta (true armyworm),Neoleucinodes elegantalis (small tomato borer), Nymphula depunctalis(rice caseworm), Operophthera brumata (winter moth), Ostrinia nubilalis(European corn borer), Oxydia vesulia, Pandemis cerasana (common curranttortrix), Pandemis heparana (brown apple tortrix), Papilio demodocus,Pectinophora gossypiella (pink bollworm), Peridroma spp. (cutworms),Peridroma saucia (variegated cutworm), Perileucoptera coffeella (whitecoffee leafminer), Phthorimaea operculella (potato tuber moth),Phyllocnisitis citrella, Phyllonorycter spp. (leafminers), Pieris rapae(imported cabbageworm), Plathypena scabra, Plodia interpunctella (Indianmeal moth), Plutella xylostella (diamondback moth), Polychrosis viteana(grape berry moth), Prays endocarpa, Prays oleae (olive moth),Pseudaletia spp. (noctuid moths), Pseudaletia unipunctata (armyworm),Pseudoplusia includens (soybean looper), Rachiplusia nu, Scirpophagaincertulas, Sesamia spp. (stemborers), Sesamia inferens (pink rice stemborer), Sesamia nonagrioides, Setora nitens, Sitotroga cerealella(Angoumois grain moth), Sparganothis pilleriana, Spodoptera spp.(armyworms), Spodoptera exigua (beet armyworm), Spodoptera fugiperda(fall armyworm), Spodoptera oridania (southern armyworm), Synanthedonspp. (root borers), Thecla basilides, Thermisia gemmatalis, Tineolabisselliella (webbing clothes moth), Trichoplusia ni (cabbage looper),Tuta absoluta, Yponomeuta spp., Zeuzera coffeae (red branch borer), andZeuzera pyrina (leopard moth).

In another embodiment, the invention disclosed in this document can beused to control Mallophaga (chewing lice). A non-exhaustive list ofthese pests includes, but is not limited to, Bovicola ovis (sheep bitinglouse), Menacanthus stramineus (chicken body louse), and Menopongallinea (common hen house).

In another embodiment, the invention disclosed in this document can beused to control Orthoptera (grasshoppers, locusts, and crickets). Anon-exhaustive list of these pests includes, but is not limited to,Anabrus simplex (Mormon cricket), Gryllotalpidae (mole crickets),Locusta migratoria, Melanoplus spp. (grasshoppers), Microcentrumretinerve (angularwinged katydid), Pterophylla spp. (kaydids),chistocerca gregaria, Scudderia furcata (forktailed bush katydid), andValanga nigricorni.

In another embodiment, the invention disclosed in this document can beused to control Phthiraptera (sucking lice). A non-exhaustive list ofthese pests includes, but is not limited to, Haematopinus spp. (cattleand hog lice), Linognathus ovillus (sheep louse), Pediculus humanuscapitis (human body louse), Pediculus humanus humanus (human body lice),and Pthirus pubis (crab louse),

In another embodiment, the invention disclosed in this document can beused to control Siphonaptera (fleas). A non-exhaustive list of thesepests includes, but is not limited to, Ctenocephalides canis (dog flea),Ctenocephalides felis (cat flea), and Pulex irritans (human flea).

In another embodiment, the invention disclosed in this document can beused to control Thysanoptera (thrips). A non-exhaustive list of thesepests includes, but is not limited to, Frankliniella fusca (tobaccothrips), Frankliniella occidentalis (western flower thrips),Frankliniella shultzei Frankliniella williamsi (corn thrips),Heliothrips haemorrhaidalis (greenhouse thrips), Riphiphorothripscruentatus, Scirtothrips spp., Scirtothrips citri (citrus thrips),Scirtothrips dorsalis (yellow tea thrips), Taeniothripsrhopalantennalis, and Thrips spp.

In another embodiment, the invention disclosed in this document can beused to control Thysanura (bristletails). A non-exhaustive list of thesepests includes, but is not limited to, Lepisma spp. (silverfish) andThermobia spp. (firebrats).

In another embodiment, the invention disclosed in this document can beused to control Acarina (mites and ticks). A non-exhaustive list ofthese pests includes, but is not limited to, Acarapsis woodi (trachealmite of honeybees), Acarus spp. (food mites), Acarus siro (grain mite),Aceria mangiferae (mango bud mite), Aculops spp., Aculops lycopersici(tomato russet mite), Aculops pelekasi, Aculus pelekassi, Aculusschlechtendali (apple rust mite), Amblyomma americanum (lone star tick),Boophilus spp. (ticks), Brevipalpus obovatus (privet mite), Brevipalpusphoenicis (red and black flat mite), Demodex spp. (mange mites),Dermacentor spp. (hard ticks), Dermacentor variabilis (american dogtick), Dermatophagoides pteronyssinus (house dust mite), Eotetranycusspp., Eotetranychus carpini (yellow spider mite), Epitimerus spp.,Eriophyes spp., Ixodes spp. (ticks), Metatetranycus spp., Notoedrescati, Oligonychus spp., Oligonychus coffee, Oligonychus ilicus (southernred mite), Panonychus spp., Panonychus citri (citrus red mite),Panonychus ulmi (European red mite), Phyllocoptruta oleivora (citrusrust mite), Polyphagotarsonemun latus (broad mite), Rhipicephalussanguineus (brown dog tick), Rhizoglyphus spp. (bulb mites), Sarcoptesscabiei (itch mite), Tegolophus perseaflorae, Tetranychus spp.,Tetranychus urticae (twospotted spider mite), and Varroa destructor(honey bee mite).

In another embodiment, the invention disclosed in this document can beused to control Nematoda (nematodes). A non-exhaustive list of thesepests includes, but is not limited to, Aphelenchoides spp. (bud and leaf& pine wood nematodes), Belonolaimus spp. (sting nematodes),Criconemella spp. (ring nematodes), Dirofilaria immitis (dog heartworm),Ditylenchus spp. (stem and bulb nematodes), Heterodera spp. (cystnematodes), Heterodera zeae (corn cyst nematode), Hirschmanniella spp.(root nematodes), Hoplolaimus spp. (lance nematodes), Meloidogyne spp.(root knot nematodes), Meloidogyne incognita (root knot nematode),Onchocerca volvulus (hook-tail worm), Pratylenchus spp. (lesionnematodes), Radopholus spp. (burrowing nematodes), and Rotylenchusreniformis (kidney-shaped nematode).

In another embodiment, the invention disclosed in this document can beused to control Symphyla (symphylans). A non-exhaustive list of thesepests includes, but is not limited to, Scutigerella immaculata.

For more detailed information consult “Handbook of Pest Control—TheBehavior, Life Histroy, and Control of Household Pests” by ArnoldMallis, 9^(th) Edition, copyright 2004 by GIE Media Inc.

Mixtures

Some of the pesticides that can be employed beneficially in combinationwith the invention disclosed in this document include, but are notlimited to the following:

1,2 dichloropropane, 1,3 dichloropropene,

abamectin, acephate, acequinocyl, acetamiprid, acethion, acetoprole,acrinathrin, acrylonitrile, alanycarb, aldicarb, aldoxycarb, aldrin,allethrin, allosamidin, allyxycarb, alpha-cypermethrin, alpha-ecdysone,alpha-endosulfan, AKD-1022, amidithion, amidoflumet, aminocarb, amiton,amitraz, anabasine, arsenous oxide, athidathion, azadirachtin,azamethiphos, azinphos ethyl, azinphos methyl, azobenzene, azocyclotin,azothoate,

Bacillus thuringiensis, barium hexafluorosilicate, barthrin,benclothiaz, bendiocarb, benfuracarb, benomyl, benoxafos, bensultap,benzoximate, benzyl benzoate, beta-cyfluthrin, beta-cypermethrin,bifenazate, bifenthrin, binapacryl, bioallethrin, bioethanomethrin,biopermethrin, bistrifluoron, borax, boric acid, bromfenvinfos, bromoDDT, bromocyclen, bromophos, bromophos ethyl, bromopropylate, bufencarb,buprofezin, butacarb, butathiofos, butocarboxim, butonate,butoxycarboxim,

cadusafos, calcium arsenate, calcium polysulfide, camphechlor,carbanolate, carbaryl, carbofuran, carbon disulfide, carbontetrachloride, carbophenothion, carbosulfan, cartap, chinomethionat,chlorantraniliprole, chlorbenside, chlorbicyclen, chlordane,chlordecone, chlordimeform, chlorethoxyfos, chlorfenapyr, chlorfenethol,chlorfenson, chlorfensulphide, chlorfenvinphos, chlorfluazuron,chlormephos, chlorobenzilate,3-(4-chloro-2,6-diemthylphenyl)-4-hydroxy-8-oxa-1-azaspiro[4,5]dec-3-en-2-one,3-(4′-chloro-2,4-dimethyl[1,1′-biphenyl]-3-yl)-4-hydroxy-8-oxa-1-azaspiro[4,5]dec-3-en-2-one,4-[[(6-chloro-3-pyridinyl)methyl]methylamino]-2(5H)-furanone,4-[[(6-chloro-3-pyridinyl)methyl]cyclopropylamino]-2(5H)-furanone,3-chloro-N2-[(1S)-1-methyl-2-(methylsulfonyl)ethyl]-N1-[2-methyl-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl]-1,2-benzenedicarboxamide,chloroform, chloromebuform, chloromethiuron, chloropicrin,chloropropylate, chlorphoxim, chlorprazophos, chlorpyrifos,chlorpyrifos-methyl, chlorthiophos, chromafenozide, cinerin I, cinerinII, cismethrin, cloethocarb, clofentezine, closantel, clothianidin,copper acetoarsenite, copper arsenate, copper naphthenate, copperoleate, coumaphos, coumithoate, crotamiton, crotoxyphos, cruentaren A &B, crufomate, cryolite, cyanofenphos, cyanophos, cyanthoate,cyanthraniliprole, cyclethrin, cycloprothrin, cyenopyrafen,cyflumetofen, cyfluthrin, cyhalothrin, cyhexatin, cypermethrin,cyphenothrin, cyromazine, cythioate,2-cyano-N-ethyl-4-fluoro-3-methoxy-benenesulfonamide,2-cyano-N-ethyl-3-methoxy-benzenesulfonamide,2-cyano-3-difluoromethoxy-N-ethyl-4-fluoro-benzenesulfonamide,2-cyano-3-fluoromethoxy-N-ethyl-benzenesulfonamide,2-cyano-6-fluoro-3-methoxy-N,N-dimethyl-benzenesulfonamide,2-cyano-N-ethyl-6-fluoro-3-methoxy-N-methyl-benzenesulfonamide,2-cyano-3-difluoromethoxy-N,N-diemthyl-benzenesulfonamide.

d-limonene, dazomet, DBCP, DCIP, DDT, decarbofuran, deltamethrin,demephion, demephion O, demephion S, demeton, demeton methyl, demeton O,demeton O methyl, demeton S, demeton S methyl, demeton S methylsulphon,diafenthiuron, dialifos, diamidafos, diazinon, dicapthon,dichlofenthion, dichlofluanid, dichlorvos, dicofol, dicresyl,dicrotophos, dicyclanil, dieldrin, dienochlor, diflovidazin,diflubenzuron,3-(difluoromethyl)-N-[2-(3,3-dimethylbutyl)phenyl]-1-methyl-1H-pyrazole-4-carboxamide,dilor, dimefluthrin, dimefox, dimetan, dimethoate, dimethrin,dimethylvinphos, dimetilan, dinex, dinobuton, dinocap, dinocap 4,dinocap 6, dinocton, dinopenton, dinoprop, dinosam, dinosulfon,dinotefuran, dinoterbon, diofenolan, dioxabenzofos, dioxacarb,dioxathion, diphenyl sulfone, disulfuram, disulfoton, dithicrofos, DNOC,dofenapyn, doramectin, ecdysterone, emamectin, EMPC, empenthrin,endosulfan, endothion, endrin, EPN, epofenonane, eprinomectin,esfenvalerate, etaphos, ethiofencarb, ethion, ethiprole, ethoate methyl,ethoprophos, ethyl DDD, ethyl formate, ethylene dibromide, ethylenedichloride, ethylene oxide, etofenprox, etoxazole, etrimfos, EXD,

F1050, famphur, fenamiphos, fenazaflor, fenazaquin, fenbutatin oxide,fenchlorphos, fenethacarb, fenfluthrin, fenitrothion, fenobucarb,fenothiocarb, fenoxacrim, fenoxycarb, fenpirithrin, fenpropathrin,fenpyroximate, fenson, fensulfothion, fenthion, fenthion ethyl,fentrifanil, fenvalerate, fipronil, FKI-1033, flonicamid, fluacrypyrim,fluazuron, flubendiamide, flubenzimine, flucofuron, flucycloxuron,flucythrinate, fluenetil, flufenerim, flufenoxuron, flufenprox,flumethrin, fluorbenside, fluvalinate, fonofos, formetanate, formothion,formparanate, fosmethilan, fospirate, fosthiazate, fosthietan,fosthietan, furathiocarb, furethrin, furfural,

gamma-cyhalothrin, gamma-HCH,

halfenprox, halofenozide, HCH, HEOD, heptachlor, heptenophos,heterophos, hexaflumuron, hexythiazox, HHDN, hydramethylnon, hydrogencyanide, hydroprene, hyquincarb,

imicyafos, imidacloprid, imidaclothiz, imiprothrin, indoxacarb,iodomethane, IPSP, isamidofos, isazofos, isobenzan, isocarbophos,isodrin, isofenphos, isoprocarb, isoprothiolane, isothioate, isoxathion,ivermectin jasmolin I, jasmolin II, jodfenphos, juvenile hormone I,juvenile hormone II, juvenile hormone III, JS118,

kelevan, kinoprene,

lambda cyhalothrin, lead arsenate, lepimectin, leptophos, lindane,lirimfos, lufenuron, lythidathion,

malathion, malonoben, mazidox, mecarbam, mecarphon, menazon,mephosfolan, mercurous chloride, mesulfen, mesulfenfos, metaflumizone,metam, methacrifos, methamidophos, methidathion, methiocarb,methocrotophos, methomyl, methoprene, methoxychlor, methoxyfenozide,methyl bromide, methyl isothiocyanate, methylchloroform, methylenechloride, metofluthrin, metolcarb, metoxadiazone, mevinphos,mexacarbate, milbemectin, milbemycin oxime, mipafox, mirex, MNAF,monocrotophos, morphothion, moxidectin,

naftalofos, naled, naphthalene, nereistoxin,N-ethyl-2,2-dimethylpropionamide-2-(2,6-dichloro-α,α,α-thrifluoro-p-tolyl)hydrazone,N-ethyl-2,2-dichloro-1-methylcyclopropane-carboxamide-2-(2,6-dichloro-α,α,α-thrifluoro-p-tolyl)hydrazone nicotine, nifluridide, nikkomycins, nitenpyram, nithiazine,nitrilacarb, novaluron, noviflumuron,

omethoate, oxamyl, oxydemeton methyl, oxydeprofos, oxydisulfoton,

paradichlorobenzene, parathion, parathion methyl, penfluoron,pentachlorophenol, pentmethrin, permethrin, phenkapton, phenothrin,phenthoate, phorate, phosalone, phosfolan, phosmet, phosnichlor,phosphamidon, phosphine, phosphocarb, phoxim, phoxim methyl, piperonylbutoxide, pirimetaphos, pirimicarb, pirimiphos ethyl, pirimiphos methyl,potassium arsenite, potassium thiocyanate, pp′ DDT, prallethrin,precocene I, precocene II, precocene III, primidophos, proclonol,profenofos, profluthrin, promacyl, promecarb, propaphos, propargite,propetamphos, propoxur, prothidathion, prothiofos, prothoate,protrifenbute, pyraclofos, pyrafluprole, pyrazophos, pyresmethrin,pyrethrin I, pyrethrin II, pyridaben, pyridalyl, pyridaphenthion,pyrifluquinazon, pyrimidifen, pyrimitate, pyriprole, pyriproxyfen,

Qcide, quassia, quinalphos, quinalphos, quinalphos methyl, quinothion,quantifies,

rafoxanide, resmethrin, rotenone, ryania,

sabadilla, schradan, selamectin, silafluofen, sodium arsenite, sodiumfluoride, sodium hexafluorosilicate, sodium thiocyanate, sophamide,spinetoram, spinosad, spirodiclofen, spiromesifen, spirotetramat,sulcofuron, sulfuram, sulfluramid, sulfotep, sulfoxaflor, sulfur,sulfuryl fluoride, sulprofos,

tau-fluvalinate, tazimcarb, TDE, tebufenozide, tebufenpyrad,tebupirimfos, teflubenzuron, tefluthrin, temephos, TEPP, terallethrin,terbufos, tetrachloroethane, tetrachlorvinphos, tetradifon,tetramethrin, tetranactin, tetrasul, theta-cypermethrin, thiacloprid,thiamethoxam, thicrofos, thiocarboxime, thiocyclam, thiodicarb,thiofanox, thiometon, thionazin, thioquinox, thiosultap, thuringiensin,tolfenpyrad, tralomethrin, transfluthrin, transpermethrin, triarathene,triazamate, triazophos, trichlorfon, trichlormetaphos 3, trichloronat,trifenofos, triflumuron, trimethacarb, triprene,

vamidothion, vaniliprole, verticilide

XDE-208, XMC, xylylcarb,

Zeta-cypermethrin and zolaprofos.

Additionally, any combination of the above pesticides can be used.

The invention disclosed in this document can also be used withherbicides and fungicides, both for reasons of economy and synergy.

The invention disclosed in this document can be used withantimicrobials, bactericides, defoliants, safeners, synergists,algaecides, attractants, desiccants, pheromones, repellants, animaldips, avicides, disinfectants, semiochemicals, and molluscicides (thesecategories not necessarily mutually exclusive) for reasons of economy,and synergy.

For more information consult “Compendium of Pesticide Common Names”located at http://www.alanwood.net/pesticides/index.html as of thefiling date of this document. Also consult “The Pesticide Manual”14^(th) Edition, edited by C D S Tomlin, copyright 2006 by British CropProduction Council.

Synergistic Mixtures

The invention disclosed in this document can be used with othercompounds such as the ones mentioned under the heading “Mixtures” toform synergistic mixtures where the mode of action of the compounds inthe mixtures are the same, similar, or different.

Examples of mode of actions include, but are not limited to: acetylcholine esterase inhibitor; sodium channel modulator; chitinbiosynthesis inhibitor; GABA-gated chloride channel antagonist; GABA andglutamate-gated chloride channel agonist; acetyl choline receptoragonist; MET I inhibitor; Mg-stimulated ATPase inhibitor; nicotinicacetylcholine receptor; Midgut membrane disrupter; and oxidativephosphorylation disrupter.

Additionally, the following compounds are known as synergists and can beused with the invention disclosed in this document: piperonyl butoxide,piprotal, propyl isome, sesamex, sesamolin, and sulfoxide.

Formulations

A pesticide is rarely suitable for application in its pure form. It isusually necessary to add other substances so that the pesticide can beused at the required concentration and in an appropriate form,permitting ease of application, handling, transportation, storage, andmaximum pesticide activity. Thus, pesticides are formulated into, forexample, baits, concentrated emulsions, dusts, emulsifiableconcentrates, fumigants, gels, granules, microencapsulations, seedtreatments, suspension concentrates, suspoemulsions, tablets, watersoluble liquids, water dispersible granules or dry flowables, wettablepowders, and ultra low volume solutions.

For further information on formulation types see “Catalogue of pesticideformulation types and international coding system” Technical Monographno 2, 5^(th) Edition by CropLife International (2002).

Pesticides are applied most often as aqueous suspensions or emulsionsprepared from concentrated formulations of such pesticides. Suchwater-soluble, water-suspendable, or emulsifiable formulations, areeither solids, usually known as wettable powders, or water dispersiblegranules, or liquids usually known as emulsifiable concentrates, oraqueous suspensions. Wettable powders, which may be compacted to formwater dispersible granules, comprise an intimate mixture of thepesticide, a carrier, and surfactants. The concentration of thepesticide is usually from about 10% to about 90% by weight. The carrieris usually chosen from among the attapulgite clays, the montmorilloniteclays, the diatomaceous earths, or the purified silicates. Effectivesurfactants, comprising from about 0.5% to about 10% of the wettablepowder, are found among sulfonated lignins, condensednaphthalenesulfonates, naphthalenesulfonates, alkylbenzenesulfonates,alkyl sulfates, and nonionic surfactants such as ethylene oxide adductsof alkyl phenols.

Emulsifiable concentrates of pesticides comprise a convenientconcentration of a pesticide, such as from about 50 to about 500 gramsper liter of liquid dissolved in a carrier that is either a watermiscible solvent or a mixture of water-immiscible organic solvent andemulsifiers. Useful organic solvents include aromatics, especiallyxylenes and petroleum fractions, especially the high-boilingnaphthalenic and olefinic portions of petroleum such as heavy aromaticnaphtha. Other organic solvents may also be used, such as the terpenicsolvents including rosin derivatives, aliphatic ketones such ascyclohexanone, and complex alcohols such as 2-ethoxyethanol. Suitableemulsifiers for emulsifiable concentrates are chosen from conventionalanionic and nonionic surfactants.

Aqueous suspensions comprise suspensions of water-insoluble pesticidesdispersed in an aqueous carrier at a concentration in the range fromabout 5% to about 50% by weight. Suspensions are prepared by finelygrinding the pesticide and vigorously mixing it into a carrier comprisedof water and surfactants. Ingredients, such as inorganic salts andsynthetic or natural gums, may also be added, to increase the densityand viscosity of the aqueous carrier. It is often most effective togrind and mix the pesticide at the same time by preparing the aqueousmixture and homogenizing it in an implement such as a sand mill, ballmill, or piston-type homogenizer.

Pesticides may also be applied as granular compositions that areparticularly useful for applications to the soil. Granular compositionsusually contain from about 0.5% to about 10% by weight of the pesticide,dispersed in a carrier that comprises clay or a similar substance. Suchcompositions are usually prepared by dissolving the pesticide in asuitable solvent and applying it to a granular carrier which has beenpre-formed to the appropriate particle size, in the range of from about0.5 to 3 mm. Such compositions may also be formulated by making a doughor paste of the carrier and compound and crushing and drying to obtainthe desired granular particle size.

Dusts containing a pesticide are prepared by intimately mixing thepesticide in powdered form with a suitable dusty agricultural carrier,such as kaolin clay, ground volcanic rock, and the like. Dusts cansuitably contain from about 1% to about 10% of the pesticide. They canbe applied as a seed dressing, or as a foliage application with a dustblower machine.

It is equally practical to apply a pesticide in the form of a solutionin an appropriate organic solvent, usually petroleum oil, such as thespray oils, which are widely used in agricultural chemistry.

Pesticides can also be applied in the form of an aerosol composition. Insuch compositions the pesticide is dissolved or dispersed in a carrier,which is a pressure-generating propellant mixture. The aerosolcomposition is packaged in a container from which the mixture isdispensed through an atomizing valve.

Pesticide baits are formed when the pesticide is mixed with food or anattractant or both. When the pests eat the bait they also consume thepesticide. Baits may take the form of granules, gels, flowable powders,liquids, or solids. They are used in pest harborages.

Fumigants are pesticides that have a relatively high vapor pressure andhence can exist as a gas in sufficient concentrations to kill pests insoil or enclosed spaces. The toxicity of the fumigant is proportional toits concentration and the exposure time. They are characterized by agood capacity for diffusion and act by penetrating the pest'srespiratory system or being absorbed through the pest's cuticle.Fumigants are applied to control stored product pests under gas proofsheets, in gas sealed rooms or buildings or in special chambers.

Pesticides can be microencapsulated by suspending the pesticideparticles or droplets in plastic polymers of various types. By alteringthe chemistry of the polymer or by changing factors in the processing,microcapsules can be formed of various sizes, solubility, wallthicknesses, and degrees of penetrability. These factors govern thespeed with which the active ingredient within is released, which. inturn, affects the residual performance, speed of action, and odor of theproduct.

Oil solution concentrates are made by dissolving pesticide in a solventthat will hold the pesticide in solution. Oil solutions of a pesticideusually provide faster knockdown and kill of pests than otherformulations due to the solvents themselves having pesticidal action andthe dissolution of the waxy covering of the integument increasing thespeed of uptake of the pesticide. Other advantages of oil solutionsinclude better storage stability, better penetration of crevices, andbetter adhesion to greasy surfaces.

Another embodiment is an oil-in-water emulsion, wherein the emulsioncomprises oily globules which are each provided with a lamellar liquidcrystal coating and are dispersed in an aqueous phase, wherein each oilyglobule comprises at least one compound which is agriculturally active,and is individually coated with a monolamellar or oligolamellar layercomprising: (1) at least one non-ionic lipophilic surface-active agent,(2) at least one non-ionic hydrophilic surface-active agent and (3) atleast one ionic surface-active agent, wherein the globules having a meanparticle diameter of less than 800 nanometers. Further information onthe embodiment is disclosed in U.S. patent publication 20070027034published Feb. 1, 2007, having patent application Ser. No. 11/495,228.For ease of use this embodiment will be referred to as “OIWE”.

For further information consult “Insect Pest Management” 2^(nd) Editionby D. Dent, copyright CAB International (2000). Additionally, for moredetailed information consult “Handbook of Pest Control—The Behavior,Life Histroy, and Control of Household Pests” by Arnold Mallis, 9^(th)Edition, copyright 2004 by GIE Media Inc.

Other Formulation Components

Generally, the invention disclosed in this document when used in aformulation, such formulation can also contain other components. Thesecomponents include, but are not limited to, (this is a non-exhaustiveand non-mutually exclusive list) wetters, spreaders, stickers,penetrants, buffers, sequestering agents, drift reduction agents,compatibility agents, anti-foam agents, cleaning agents, andemulsifiers. A few components are described forthwith.

A wetting agent is a substance that when added to a liquid increases thespreading or penetration power of the liquid by reducing the interfacialtension between the liquid and the surface on which it is spreading.Wetting agents are used for two main functions in agrochemicalformulations: during processing and manufacture to increase the rate ofwetting of powders in water to make concentrates for soluble liquids orsuspension concentrates; and during mixing of a product with water in aspray tank to reduce the wetting time of wettable powders and to improvethe penetration of water into water-dispersible granules. Examples ofwetting agents used in wettable powder, suspension concentrate, andwater-dispersible granule formulations are: sodium lauryl sulphate;sodium dioctyl sulphosuccinate; alkyl phenol ethoxylates; and aliphaticalcohol ethoxylates.

A dispersing agent is a substance which adsorbs onto the surface of aparticles and helps to preserve the state of dispersion of the particlesand prevents them from reaggregating. Dispersing agents are added toagrochemical formulations to facilitate dispersion and suspension duringmanufacture, and to ensure the particles redisperse into water in aspray tank. They are widely used in wettable powders, suspensionconcentrates and water-dispersible granules. Surfactants that are usedas dispersing agents have the ability to adsorb strongly onto a particlesurface and provide a charged or steric barrier to reaggregation ofparticles. The most commonly used surfactants are anionic, non-ionic, ormixtures of the two types. For wettable powder formulations, the mostcommon dispersing agents are sodium lignosulphonates. For suspensionconcentrates, very good adsorption and stabilization are obtained usingpolyelectrolytes, such as sodium naphthalene sulphonate formaldehydecondensates. Tristyrylphenol ethoxylate phosphate esters are also used.Non-ionics such as alkylarylethylene oxide condensates and EO-PO blockcopolymers are sometimes combined with anionics as dispersing agents forsuspension concentrates, In recent years, new types of very highmolecular weight polymeric surfactants have been developed as dispersingagents. These have very long hydrophobic ‘backbones’ and a large numberof ethylene oxide chains forming the ‘teeth’ of a ‘comb’ surfactant.These high molecular weight polymers can give very good long-termstability to suspension concentrates because the hydrophobic backboneshave many anchoring points onto the particle surfaces. Examples ofdispersing agents used in agrochemical formulations are: sodiumlignosulphonates; sodium naphthalene sulphonate formaldehydecondensates; tristyrylphenol ethoxylate phosphate esters; aliphaticalcohol ethoxylates; alky ethoxylates; EO-PO block copolymers; and graftcopolymers.

An emulsifying agent is a substance which stabilizes a suspension ofdroplets of one liquid phase in another liquid phase. Without theemulsifying agent the two liquids would separate into two immiscibleliquid phases. The most commonly used emulsifier blends containalkylphenol or aliphatic alcohol with 12 or more ethylene oxide unitsand the oil-soluble calcium salt of dodecylbenzene sulphonic acid. Arange of hydrophile-lipophile balance (“HLB”) values from 8 to 18 willnormally provide good stable emulsions. Emulsion stability can sometimesbe improved by the addition of a small amount of an EO-PO blockcopolymer surfactant.

A solubilizing agent is a surfactant which will form micelles in waterat concentrations above the critical micelle concentration. The micellesare then able to dissolve or solubilized water-insoluble materialsinside the hydrophobic part of the micelle. The type of surfactantsusually used for solubilization are non-ionics: sorbitan monooleates;sorbitan monooleate ethoxylates; and methyl oleate esters.

Surfactants are sometimes used, either alone or with other additivessuch as mineral or vegetable oils as adjuvants to spray-tank mixes toimprove the biological performance of the pesticide on the target. Thetypes of surfactants used for bioenhancement depend generally on thenature and mode of action of the pesticide. However, they are oftennon-ionics such as: alky ethoxylates; linear aliphatic alcoholethoxylates; aliphatic amine ethoxylates.

A carrier or diluent in an agricultural formulation is a material addedto the pesticide to give a product of the required strength. Carriersare usually materials with high absorptive capacities, while diluentsare usually materials with low absorptive capacities. Carriers anddiluents are used in the formulation of dusts, wettable powders,granules and water-dispersible granules.

Organic solvents are used mainly in the formulation of emulsifiableconcentrates, ULV formulations, and to a lesser extent granularformulations. Sometimes mixtures of solvents are used. The first maingroups of solvents are aliphatic paraffinic oils such as kerosene orrefined paraffins. The second main group and the most common comprisesthe aromatic solvents such as xylene and higher molecular weightfractions of C₉ and C₁₀ aromatic solvents. Chlorinated hydrocarbons areuseful as cosolvents to prevent crystallization of pesticides when theformulation is emulsified into water. Alcohols are sometimes used ascosolvents to increase solvent power.

Thickeners or gelling agents are used mainly in the formulation ofsuspension concentrates, emulsions and suspoemulsions to modify therheology or flow properties of the liquid and to prevent separation andsettling of the dispersed particles or droplets. Thickening, gelling,and anti-settling agents generally fall into two categories, namelywater-insoluble particulates and water-soluble polymers. It is possibleto produce suspension concentrate formulations using clays and silicas.Examples of these types of materials, include, but are limited to,montmorillonite, e.g. bentonite; magnesium aluminum silicate; andattapulgite. Water-soluble polysaccharides have been used asthickening-gelling agents for many years. The types of polysaccharidesmost commonly used are natural extracts of seeds and seaweeds or aresynthetic derivatives of cellulose. Examples of these types of materialsinclude, but are not limited to, guar gum; locust bean gum; carrageenam;alginates; methyl cellulose; sodium carboxymethyl cellulose (SCMC);hydroxyethyl cellulose (HEC). Other types of anti-settling agents arebased on modified starches, polyacrylates, polyvinyl alcohol andpolyethylene oxide. Another good anti-settling agent is xanthan gum.

Microorganisms cause spoilage of formulated products. Thereforepreservation agents are used to eliminate or reduce their effect.Examples of such agents include, but are limited to: propionic acid andits sodium salt; sorbic acid and its sodium or potassium salts; benzoicacid and its sodium salt; p-hydroxy benzoic acid sodium salt; methylp-hydroxy benzoate; and 1,2-benzisothiazalin-3-one (BIT).

The presence of surfactants, which lower interfacial tension, oftencauses water-based formulations to foam during mixing operations inproduction and in application through a spray tank. In order to reducethe tendency to foam, anti-foam agents are often added either during theproduction stage or before filling into bottles. Generally, there aretwo types of anti-foam agents, namely silicones and non-silicones.Silicones are usually aqueous emulsions of dimethyl polysiloxane whilethe non-silicone anti-foam agents are water-insoluble oils, such asoctanol and nonanol, or silica. In both cases, the function of theanti-foam agent is to displace the surfactant from the air-waterinterface.

For further information see “Chemistry and Technology of AgrochemicalFormulations” edited by D. A. Knowles, copyright 1998 by Kluwer AcademicPublishers. Also see “Insecticides in Agriculture andEnvironment—Retrospects and Prospects” by A. S. Perry, I. Yamamoto, I.Ishaaya, and R. Perry, copyright 1998 by Springer-Verlag.

Applications

The actual amount of pesticide to be applied to loci of pests is notcritical and can readily be determined by those skilled in the art. Ingeneral, concentrations from about 0.01 grams of pesticide per hectareto about 5000 grams of pesticide per hectare are expected to providegood control.

The locus to which a pesticide is applied can be any locus inhabited byan pest, for example, vegetable crops, fruit and nut trees, grape vines,ornamental plants, domesticated animals, the interior or exteriorsurfaces of buildings, and the soil around buildings.

Generally, with baits, the baits are placed in the ground where, forexample, termites can come into contact with the bait. Baits can also beapplied to a surface of a building, (horizontal, vertical, or slant,surface) where, for example, ants, termites, cockroaches, and flies, cancome into contact with the bait.

Because of the unique ability of the eggs of some pests to resistpesticides repeated applications may be desirable to control newlyemerged larvae.

Systemic movement of pesticides in plants may be utilized to controlpests on one portion of the plant by applying the pesticides to adifferent portion of the plant. For example, control of foliar-feedinginsects can be controlled by drip irrigation or furrow application, orby treating the seed before planting. Seed treatment can be applied toall types of seeds, including those from which plants geneticallytransformed to express specialized traits will germinate. Representativeexamples include seeds or plants expressing proteins and/or doublestranded RNA toxic to invertebrate pests, such as Bacillusthuringiensis, Bt Cry toxins, Bt Vip toxins, RNAi, or other insecticidaltoxins, those expressing herbicide resistance, such as “Roundup Ready”seed, or those with “stacked” foreign genes expressing insecticidaltoxins, herbicide resistance, nutrition-enhancement or any otherbeneficial traits. Furthermore, such seed treatments with the inventiondisclosed in this document can further enhance the ability of a plant tobetter withstand stressful growing conditions. This results in ahealthier, more vigorous plant, which can lead to higher yields atharvest time.

It should be readily apparent that the invention can be used with plantsgenetically transformed to express specialized traits, such as Bacillusthuringiensis, RNAi, or other insecticidal toxins, or those expressingherbicide resistance, or those with “stacked” foreign genes expressinginsecticidal toxins, herbicide resistance, nutrition-enhancement or anyother beneficial traits.

The invention disclosed in this document is suitable for controllingendoparasites and ectoparasites in the veterinary medicine sector or inthe field of animal keeping (which for the avoidance of doubt includespets, for example, cats, dogs, and birds). Compounds according to theinvention are applied here in a known manner, such as by oraladministration in the form of, for example, tablets, capsules, drinks,granules, by dermal application in the form of, for example, dipping,spraying, pouring on, spotting on, and dusting, and by parenteraladministration in the form of, for example, an injection.

The invention disclosed in this document can also be employedadvantageously in livestock keeping, for example, cattle, sheep, pigs,chickens, and geese. Suitable formulations are administered orally tothe animals with the drinking water or feed. The dosages andformulations that are suitable depend on the species.

Before a pesticide can be used or sold commercially, such pesticideundergoes lengthy evaluation processes by various governmentalauthorities (local, regional, state, national, international).Voluminous data requirements are specified by regulatory authorities andmust be addressed through data generation and submission by the productregistrant or by another on the product registrant's behalf. Thesegovernmental authorities then review such data and if a determination ofsafety is concluded, provide the potential user or seller with productregistration approval. Thereafter, in that locality where the productregistration is granted and supported, such user or seller may use orsell such pesticide.

The headings in this document are for convenience only and must not beused to interpret any portion thereof.

For the avoidance of doubt Ar1 is sometimes referred to as Ar1 fortypographic and formatting reasons. Additionally, Ar2 is sometimesreferred to as Ar2 for typographic and formatting reasons. For thepurposes of this invention the saturation of a double or triple bondwith other atoms is considered a substitution.

1. A compound having the following formula:

wherein: (a) Ar₁ is (1) furanyl, phenyl, pyridazinyl, pyridyl,pyrimidinyl, thienyl, or (2) substituted furanyl, substituted phenyl,substituted pyridazinyl, substituted pyridyl, substituted pyrimidinyl,or substituted thienyl, wherein said substituted furanyl, substitutedphenyl, substituted pyridazinyl, substituted pyridyl, substitutedpyrimidinyl, and substituted thienyl, have one or more substituentsindependently selected from H, OH, F, Cl, Br, I, CN, NO₂, C₁-C₆ alkyl,C₁-C₆ haloalkyl, C₁-C₆ hydroxyalkyl, C₃-C₆ cycloalkyl, C₃-C₆halocycloalkyl, C₃-C₆ hydroxycycloalkyl, C₃-C₆ cycloalkoxy, C₃-C₆halocycloalkoxy, C₃-C₆ hydroxycycloalkoxy, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₂-C₆ alkenyl, C₂-C₆ alkynyl, S(═O)_(n)(C₁-C₆ alkyl),S(═O)_(n)(C₁-C₆ haloalkyl), OSO₂(C₁-C₆ alkyl), OSO₂(C₁-C₆ haloalkyl),C(═O)H, C(═O)OH, C(═O)NR_(x)R_(y), (C₁-C₆ alkyl)NR_(x)R_(y), C(═O)(C₁-C₆alkyl), C(═O)O(C₁-C₆ alkyl), C(═O)(C₁-C₆ haloalkyl), C(═O)O(C₁-C₆haloalkyl), C(═O)(C₃-C₆ cycloalkyl), C(═O)O(C₃-C₆ cycloalkyl),C(═O)(C₂-C₆ alkenyl), C(═O)O(C₂-C₆ alkenyl), (C₁-C₆ alkyl)O(C₁-C₆alkyl), (C₁-C₆ alkyl)S(C₁-C₆ alkyl), C(═O)(C₁-C₆ alkyl)C(═O)O(C₁-C₆alkyl), phenyl, phenoxy, substituted phenyl and substituted phenoxy(wherein such substituted phenyl and substituted phenoxy have one ormore substituents independently selected from H, OH, F, Cl, Br, I, CN,NO₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ hydroxyalkyl, C₃-C₆ cycloalkyl,C₃-C₆ halocycloalkyl, C₃-C₆ hydroxycycloalkyl, C₃-C₆ cycloalkoxy, C₃-C₆halocycloalkoxy, C₃-C₆ hydroxycycloalkoxy, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₂-C₆ alkenyl, C₂-C₆ alkynyl, S(═O)_(n)(C₁-C₆ alkyl),S(═O)_(n)(C₁-C₆ haloalkyl), OSO₂(C₁-C₆ alkyl), OSO₂(C₁-C₆ haloalkyl),C(═O)H, C(═O)OH, C(═O)NR_(x)R_(y), (C₁-C₆ alkyl)NR_(x)R_(y, C(═O)(C)₁-C₆ alkyl), C(═O)O(C₁-C₆ alkyl), C(═O)(C₁-C₆ haloalkyl), C(═O)O(C₁-C₆haloalkyl), C(═O)(C₃-C₆ cycloalkyl), C(═O)O(C₃-C₆ cycloalkyl),C(═O)(C₂-C₆ alkenyl), C(═O)O(C₂-C₆ alkenyl), (C₁-C₆ alkyl)O(C₁-C₆alkyl), (C₁-C₆ alkyl)S(C₁-C₆ alkyl), C(═O)(C₁-C₆ alkyl)C(═O)O(C₁-C₆alkyl)phenyl, and phenoxy); (b) Het is a 5 or 6 membered, saturated orunsaturated, heterocyclic ring, containing one or more heteroatomsindependently selected from nitrogen, sulfur, or oxygen, and where Ar₁and Ar₂ are not ortho to each other (but may be meta or para, such as,for a five membered ring they are 1,3 and for a 6 membered ring they areeither 1,3 or 1,4), and where said heterocyclic ring may also besubstituted with one or more substituents independently selected from H,OH, F, Cl, Br, I, CN, NO₂, oxo, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆hydroxyalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₃-C₆hydroxycycloalkyl, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₃-C₆hydroxycycloalkoxy, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₆ alkenyl, C₂-C₆alkynyl, S(═O)_(n)(C₁-C₆ alkyl), S(═O)_(n)(C₁-C₆ haloalkyl), OSO₂(C₁-C₆alkyl), OSO₂(C₁-C₆ haloalkyl), C(═O)H, C(═O)OH, C(═O)NR_(x)R_(y), (C₁-C₆alkyl)NR_(x)R_(y), C(═O)(C₁-C₆ alkyl), C(═O)O(C₁-C₆ alkyl), C(═O)(C₁-C₆haloalkyl), C(═O)O(C₁-C₆ haloalkyl), C(═O)(C₃-C₆ cycloalkyl),C(═O)O(C₃-C₆ cycloalkyl), C(═O)(C₂-C₆ alkenyl), C(═O)O(C₂-C₆ alkenyl),(C₁-C₆ alkyl)O(C₁-C₆ alkyl), (C₁-C₆ alkyl)S(C₁-C₆ alkyl), C(═O)(C₁-C₆alkyl)C(═O)O(C₁-C₆ alkyl), phenyl, phenoxy, substituted phenyl andsubstituted phenoxy (wherein such substituted phenyl and substitutedphenoxy have one or more substituents independently selected from H, OH,F, Cl, Br, I, CN, NO₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ hydroxyalkyl,C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₃-C₆ hydroxycycloalkyl, C₃-C₆cycloalkoxy, C₃-C₆ halocycloalkoxy, C₃-C₆ hydroxycycloalkoxy, C₁-C₆alkoxy, C₁-C₆ haloalkoxy, C₂-C₆ alkenyl, C₂-C₆ alkynyl, S(═O)_(n)(C₁-C₆alkyl), S(═O)_(n)(C₁-C₆ haloalkyl), OSO₂(C₁-C₆ alkyl), OSO₂(C₁-C₆haloalkyl), C(═O)H, C(═O)OH, C(═O)NR_(x)R_(y), (C₁-C₆ alkyl)NR_(x)R_(y),C(═O)(C₁-C₆ alkyl), C(═O)O(C₁-C₆ alkyl), C(═O)(C₁-C₆ haloalkyl),C(═O)O(C₁-C₆ haloalkyl), C(═O)(C₃-C₆ cycloalkyl), C(═O)O(C₃-C₆cycloalkyl), C(═O)(C₂-C₆ alkenyl), C(═O)O(C₂-C₆ alkenyl), (C₁-C₆alkyl)O(C₁-C₆ alkyl), (C₁-C₆ alkyl)S(C₁-C₆ alkyl), C(═O)(C₁-C₆alkyl)C(═O)O(C₁-C₆ alkyl), phenyl, and phenoxy); (c) Ar₂ is (1) furanyl,phenyl, pyridazinyl, pyridyl, pyrimidinyl, thienyl, or (2) substitutedfuranyl, substituted phenyl, substituted pyridazinyl, substitutedpyridyl, substituted pyrimidinyl, or substituted thienyl, wherein saidsubstituted furanyl, substituted phenyl, substituted pyridazinyl,substituted pyridyl, substituted pyrimidinyl, and substituted thienyl,have one or more substituents independently selected from H, OH, F, Cl,Br, I, CN, NO₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ hydroxyalkyl, C₃-C₆cycloalkyl, C₃-C₆ halocycloalkyl, C₃-C₆ hydroxycycloalkyl, C₃-C₆cycloalkoxy, C₃-C₆ halocycloalkoxy, C₃-C₆ hydroxycycloalkoxy, C₁-C₆alkoxy, C₁-C₆ haloalkoxy, C₂-C₆ alkenyl, C₂-C₆ alkynyl, S(═O)_(n)(C₁-C₆alkyl), S(═O)_(n)(C₁-C₆ haloalkyl), OSO₂(C₁-C₆ alkyl), OSO₂(C₁-C₆haloalkyl), C(═O)H, C(═O)OH, C(═O)NR_(x)R_(y), (C₁-C₆ alkyl)NR_(x)R_(y),C(═O)(C₁-C₆ alkyl), C(═O)O(C₁-C₆ alkyl), C(═O)(C₁-C₆ haloalkyl),C(═O)O(C₁-C₆ haloalkyl), C(═O)(C₃-C₆ cycloalkyl), C(═O)O(C₃-C₆cycloalkyl), C(═O)(C₂-C₆ alkenyl), C(═O)O(C₂-C₆ alkenyl), (C₁-C₆alkyl)O(C₁-C₆ alkyl), (C₁-C₆ alkyl)S(C₁-C₆ alkyl), C(═O)(C₁-C₆alkyl)C(═O)O(C₁-C₆ alkyl), phenyl, phenoxy, substituted phenyl andsubstituted phenoxy (wherein such substituted phenyl and substitutedphenoxy have one or more substituents independently selected from H, OH,F, Cl, Br, I, CN, NO₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ hydroxyalkyl,C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₃-C₆ hydroxycycloalkyl, C₃-C₆cycloalkoxy, C₃-C₆ halocycloalkoxy, C₃-C₆ hydroxycycloalkoxy, C₁-C₆alkoxy, C₁-C₆ haloalkoxy, C₂-C₆ alkenyl, C₂-C₆ alkynyl, S(═O)_(n)(C₁-C₆alkyl), S(═O)_(n)(C₁-C₆ haloalkyl), OSO₂(C₁-C₆ alkyl), OSO₂(C₁-C₆haloalkyl), C(═O)H, C(═O)OH, C(═O)NR_(x)R_(y), (C₁-C₆ alkyl)NR_(x)R_(y),C(═O)(C₁-C₆ alkyl), C(═O)O(C₁-C₆ alkyl), C(═O)(C₁-C₆ haloalkyl),C(═O)O(C₁-C₆ haloalkyl), C(═O)(C₃-C₆ cycloalkyl), C(═O)O(C₃-C₆cycloalkyl), C(═O)(C₁-C₆ haloalkyl), C(═O)(C₂-C₆ alkenyl), C(═O)O(C₂-C₆alkenyl), (C₁-C₆ alkyl)O(C₁-C₆ alkyl), (C₁-C₆ alkyl)S(C₁-C₆ alkyl),C(═O)(C₁-C₆ alkyl)C(═O)O(C₁-C₆ alkyl), phenyl, and phenoxy); (d) J is O,N, NR5, CR5, C═O, or J and Ar₂ form a 3, 4, 5, or 6 membered ring; (e) Lis a single or double bond; (f) K is CR5, C═O, N, NR5, or C═S; (g) Q isO or S; (h) R1 is H, OH, F, Cl, Br, I, oxo, C₁-C₆ alkyl, C₁-C₆haloalkyl, C₁-C₆ alkoxy, C₃-C₆ cycloalkoxy, C₁-C₆ haloalkoxy, C₂-C₆alkenyloxy, (C₁-C₆ alkyl)O(C₁-C₆ alkyl), (C₁-C₆ alkyl)O(C₁-C₆ alkoxy),OC(═O)(C₁-C₆ alkyl), OC(═O)(C₃-C₆ cycloalkyl), OC(═O)(C₁-C₆ haloalkyl),OC(═O)(C₂-C₆ alkenyl), or NR_(x)R_(y); (i) R2 is H, OH, F, Cl, Br, I,oxo, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₃-C₆ cycloalkoxy,C₁-C₆ haloalkoxy, C₂-C₆ alkenyloxy, (C₁-C₆ alkyl)O(C₁-C₆ alkyl), (C₁-C₆alkyl)O(C₁-C₆ alkoxy), OC(═O)(C₁-C₆ alkyl), OC(═O)(C₃-C₆ cycloalkyl),OC(═O)(C₁-C₆ haloalkyl), OC(═O)(C₂-C₆ alkenyl), or NR_(x)R_(y); (j) R3is H, OH, F, Cl, Br, I, oxo, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy,C₃-C₆ cycloalkoxy, C₁-C₆ haloalkoxy, C₂-C₆ alkenyloxy, (C₁-C₆alkyl)O(C₁-C₆ alkyl), (C₁-C₆ alkyl)O(C₁-C₆ alkoxy), OC(═O)(C₁-C₆ alkyl),OC(═O)(C₃-C₆ cycloalkyl), OC(═O)(C₁-C₆ haloalkyl), OC(═O)(C₂-C₆alkenyl), or NR_(x)R_(y); (k) R4 is H, C₁-C₆ alkyl, C₁-C₆ haloalkyl,C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₆ alkenyloxy, (C₁-C₆ alkyl)O(C₁-C₆alkyl); and (l) R5 is H, OH, F, Cl, Br, I, CN, NO₂, C₁-C₆ alkyl, C₁-C₆haloalkyl, C₁-C₆ hydroxyalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl,C₃-C₆ hydroxycycloalkyl, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₃-C₆hydroxycycloalkoxy, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₆ alkenyl, C₂-C₆alkynyl, S(═O)_(n)(C₁-C₆ alkyl), S(═O)_(n)(C₁-C₆ haloalkyl), OSO₂(C₁-C₆alkyl), OSO₂(C₁-C₆ haloalkyl), C(═O)H, C(═O)OH, C(═O)NR_(x)R_(y), (C₁-C₆alkyl)NR_(x)R_(y), C(═O)(C₁-C₆ alkyl), C(═O)O(C₁-C₆ alkyl), C(═O)(C₁-C₆haloalkyl), C(═O)O(C₁-C₆ haloalkyl), C(═O)(C₃-C₆ cycloalkyl),C(═O)O(C₃-C₆ cycloalkyl), C(═O)(C₂-C₆ alkenyl), C(═O)O(C₂-C₆ alkenyl),(C₁-C₆ alkyl)O(C₁-C₆ alkyl), (C₁-C₆ alkyl)S(C₁-C₆ alkyl), C(═O)(C₁-C₆alkyl)C(═O)O(C₁-C₆ alkyl), phenyl, phenoxy, wherein each alkyl,haloalkyl, hydroxyalkyl, cycloalkyl, halocycloalkyl, hydroxycycloalkyl,cycloalkoxy, halocycloalkoxy, hydroxycycloalkoxy, alkoxy, haloalkoxy,alkenyl, alkynyl, phenyl, and phenoxy are optionally substituted withone or more substituents independently selected from OH, F, Cl, Br, I,CN, NO₂, oxo, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ hydroxyalkyl, C₃-C₆cycloalkyl, C₃-C₆ halocycloalkyl, C₃-C₆ hydroxycycloalkyl, C₃-C₆cycloalkoxy, C₃-C₆ halocycloalkoxy, C₃-C₆ hydroxycycloalkoxy, C₁-C₆alkoxy, C₁-C₆ haloalkoxy, C₂-C₆ alkenyl, C₂-C₆ alkynyl, S(═O)_(n)(C₁-C₆alkyl), S(═O)_(n)(C₁-C₆ haloalkyl), OSO₂(C₁-C₆ alkyl), OSO₂(C₁-C₆haloalkyl), C(═O)H, C(═O)OH, C(═O)NR_(x)R_(y), (C₁-C₆ alkyl)NR_(x)R_(y),C(═O)(C₁-C₆ alkyl), C(═O)O(C₁-C₆ alkyl), C(═O)(C₁-C₆ haloalkyl),C(═O)O(C₁-C₆ haloalkyl), C(═O)(C₃-C₆ cycloalkyl), C(═O)O(C₃-C₆cycloalkyl), C(═O)(C₂-C₆ alkenyl), C(═O)O(C₂-C₆ alkenyl), (C₁-C₆alkyl)O(C₁-C₆ alkyl), (C₁-C₆ alkyl)S(C₁-C₆ alkyl), C(═O)(C₁-C₆alkyl)C(═O)O(C₁-C₆ alkyl), phenyl, and phenoxy; (m) n=0, 1, or 2; (n)R_(x) and R_(y) are independently selected from H, C₁-C₆ alkyl, C₁-C₆haloalkyl, C₁-C₆ hydroxyalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl,C₃-C₆ hydroxycycloalkyl, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₃-C₆hydroxycycloalkoxy, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₆ alkenyl, C₂-C₆alkynyl, S(═O)_(n)(C₁-C₆ alkyl), S(═O)_(n)(C₁-C₆ haloalkyl), OSO₂(C₁-C₆alkyl), OSO₂(C₁-C₆ haloalkyl), C(═O)H, C(═O)OH, C(═O)(C₁-C₆ alkyl),C(═O)O(C₁-C₆ alkyl), C(═O)(C₁-C₆ haloalkyl), C(═O)O(C₁-C₆ haloalkyl),C(═O)(C₃-C₆ cycloalkyl), C(═O)O(C₃-C₆ cycloalkyl), C(═O)(C₂-C₆ alkenyl),C(═O)O(C₂-C₆ alkenyl), (C₁-C₆ alkyl)O(C₁-C₆ alkyl), (C₁-C₆ alkyl)S(C₁-C₆alkyl), C(═O)(C₁-C₆ alkyl)C(═O)O(C₁-C₆ alkyl), phenyl, and phenoxy.
 2. Acompound according to claim 1 wherein: Ar₁ is substituted phenyl whereinsaid substituted phenyl has one or more substituents independentlyselected from F, Cl, Br, I, C₁-C₆ alkyl, C₁-C₆ haloalkyl, and C₁-C₆haloalkoxy.
 3. A compound according to claim 1 wherein: Het isimidazolyl, isothiazolyl, isoxazolyl, 1,2,4-oxadiazolyl,1,3,4-oxadiazolyl, oxazolinyl, oxazolyl, piperazinyl, piperidinyl,pyrazinyl, pyrazolinyl, pyrazolyl, pyridazinyl, pyridyl, pyrimidinyl,pyrrolyl, 1,2,3,4-tetrazolyl, thiadiazolyl, thiazolinyl, thiazolyl,1,2,3-triazinyl, 1,2,4-triazinyl, 1,3,5-triazinyl, 1,2,3-triazolyl,1,2,4-triazolyl, substituted imidazolyl, substituted isothiazolyl,substituted isoxazolyl, substituted 1,2,4-oxadiazolyl, substituted 1,3,4oxadiazolyl, substituted oxazolinyl, substituted oxazolyl, substitutedpiperazinyl, substituted piperidinyl, substituted pyrazinyl, substitutedpyrazolinyl, substituted pyrazolyl, substituted pyridazinyl, substitutedpyridyl, substituted pyrimidinyl, substituted pyrrolyl, substitutedtetrazolyl, substituted thiadiazolyl, substituted thiazolinyl,substituted thiazolyl, substituted 1,2,3-triazinyl, substituted1,2,4-triazinyl, substituted 1,3,5-triazinyl, substituted1,2,3-triazolyl, and substituted 1,2,4-triazolyl, where said substitutedgroups have one or more substituents independently selected from H, OH,F, Cl, Br, I, CN, NO₂, oxo, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆hydroxyalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₃-C₆hydroxycycloalkyl, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₃-C₆hydroxycycloalkoxy, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₆ alkenyl, C₂-C₆alkynyl, S(═O)_(n)(C₁-C₆ alkyl), S(═O)_(n)(C₁-C₆ haloalkyl), OSO₂(C₁-C₆alkyl), OSO₂(C₁-C₆ haloalkyl), C(═O)H, C(═O)OH, C(═O)NR_(x)R_(y), (C₁-C₆alkyl)NR_(x)R_(y), C(═O)(C₁-C₆ alkyl), C(═O)O(C₁-C₆ alkyl), C(═O)(C₁-C₆haloalkyl), C(═O)(C₃-C₆ cycloalkyl), C(═O)O(C₃-C₆ cycloalkyl),C(═O)(C₁-C₆ haloalkyl), C(═O)(C₂-C₆ alkenyl), C(═O)O(C₂-C₆ alkenyl),(C₁-C₆ alkyl)O(C₁-C₆ alkyl), (C₁-C₆ alkyl)S(C₁-C₆ alkyl), C(═O)(C₁-C₆alkyl)C(═O)O(C₁-C₆ alkyl)phenyl, phenoxy, substituted phenyl andsubstituted phenoxy (wherein such substituted phenyl and substitutedphenoxy have one or more substituents independently selected from H, OH,F, Cl, Br, I, CN, NO₂, oxo, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆hydroxyalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₃-C₆hydroxycycloalkyl, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₃-C₆hydroxycycloalkoxy, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₆ alkenyl, C₂-C₆alkynyl, S(═O)_(n)(C₁-C₆ alkyl), S(═O)_(n)(C₁-C₆ haloalkyl), OSO₂(C₁-C₆alkyl), OSO₂(C₁-C₆ haloalkyl), C(═O)H, C(═O)OH, C(═O)NR_(x)R_(y), (C₁-C₆alkyl)NR_(x)R_(y), C(═O)(C₁-C₆ alkyl), C(═O)O(C₁-C₆ alkyl), C(═O)(C₁-C₆haloalkyl), C(═O)(C₃-C₆ cycloalkyl), C(═O)O(C₃-C₆ cycloalkyl),C(═O)(C₁-C₆ haloalkyl), C(═O)(C₂-C₆ alkenyl), C(═O)O(C₂-C₆ alkenyl),(C₁-C₆ alkyl)O(C₁-C₆ alkyl), (C₁-C₆ alkyl)S(C₁-C₆ alkyl), C(═O)(C₁-C₆alkyl)C(═O)O(C₁-C₆ alkyl)phenyl, and phenoxy).
 4. A compound accordingto claim 1 wherein: Het is imidazolyl, isoxazolyl, 1,2,4-oxadiazolyl,pyrazinyl, pyrimidinyl, thiazolyl, 1,3,5-triazinyl, 1,2,4-triazolyl,substituted imidazolyl, substituted pyrazolyl, and substituted1,2,4-triazolyl, where said substituted groups have one or moresubstituents independently selected from oxo, C₁-C₆ alkyl, C₁-C₆haloalkyl, C₂-C₆ alkenyl, and C(═O)O(C₁-C₆ alkyl).
 5. A compoundaccording to claim 1 wherein: Ar₂ is substituted phenyl wherein saidsubstituted phenyl has one or more substituents independently selectedfrom F, Cl, Br, I, C₁-C₆ alkyl, C₁-C₆ haloalkyl, and C₁-C₆ alkoxy.
 6. Acompound according to claim 1 wherein: R5 is H, C₁-C₆ alkyl, C₁-C₆haloalkyl, C₁-C₆ hydroxyalkyl, C₂-C₆ alkenyl, C(═O)(C₁-C₆ alkyl), (C₁-C₆alkyl)O(C₁-C₆ alkyl), and C(═O)(C₁-C₆ alkyl)C(═O)O(C₁-C₆ alkyl).
 7. Acompound that is a pesticidally acceptable acid addition salt of acompound according to claim
 1. 8. A solvate comprising compoundaccording to claim
 1. 9. A process comprising applying a compoundaccording to claim 1 to a locus to control pests.
 10. A processcomprising applying a compound according to claim 1 to a locus tocontrol pests of Phylum Nematoda or Phylum Arthropoda.
 11. A compositioncomprising a mixture of a compound according to claim 1 with at leastone other pesticide.
 12. A composition comprising a mixture of acompound according to claim 1 with at least one other compound selectedfrom antibiotic insecticides, macrocyclic lactone insecticides,avermectin insecticides, milbemycin insecticides, spinosyn insecticides,arsenical insecticides, botanical insecticides, carbamate insecticides,benzofuranyl methylcarbamate insecticides, dimethylcarbamateinsecticides, oxime carbamate insecticides, phenyl methylcarbamateinsecticides, diamide insecticides, desiccant insecticides,dinitrophenol insecticides, fluorine insecticides, formamidineinsecticides, fumigant insecticides, inorganic insecticides, insectgrowth regulators, chitin synthesis inhibitors, juvenile hormone mimics,juvenile hormones, moulting hormone agonists, moulting hormones,moulting inhibitors, precocenes, nereistoxin analogue insecticides,nicotinoid insecticides, nitroguanidine insecticides, nitromethyleneinsecticides, pyridylmethylamine insecticides, organochlorineinsecticides, organophosphorus insecticides, oxadiazine insecticides,oxadiazolone insecticides, phthalimide insecticides, pyrazoleinsecticides, pyrethroid insecticides, pyrimidinamine insecticides,pyrrole insecticides, tetramic acid insecticides, tetronic acidinsecticides, thiazole insecticides, thiazolidine insecticides, thioureainsecticides, sulfoximine insecticides, and urea insecticides.
 13. Aprocess of applying a compound according to claim 1 to a seed.
 14. Aprocess of applying a compound of claim 1 to a seed that has beengenetically transformed to express one or more specialized traits.
 15. Aprocess of applying a compound of claim 1 to a genetically transformedplant that has been genetically transformed to express one or morespecialized traits.
 16. A process of orally administering or applying acompound of claim 1 to an animal.
 17. A process comprising submittingdata relating to a compound of claim 1 to a governmental authority inorder to obtain product registration approval for a product comprising acompound of claim
 1. 18. A compound having the following formula:

wherein: (a) Ar₁ is furanyl, phenyl, pyridazinyl, pyridyl, pyrimidinyl,thienyl, substituted furanyl, substituted phenyl, substitutedpyridazinyl, substituted pyridyl, substituted pyrimidinyl, orsubstituted thienyl, wherein said substituted furanyl, substitutedphenyl, substituted pyridazinyl, substituted pyridyl, substitutedpyrimidinyl, and substituted thienyl, have one or more substituentsindependently selected from H, F, Cl, Br, I, CN, NO₂, oxo, C₁-C₆ alkyl,C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkyl, C₁-C₆haloalkoxy, S(═O)_(n)C₁-C₆ alkyl (where n=0-2), S(═O)_(n)C₁-C₆ haloalkyl(where n=0-2), OSO₂C₁-C₆ haloalkyl, C(═O)OC₁-C₆ alkyl, C(═O)C₁-C₆ alkyl,C(═O)C₁-C₆ haloalkyl, phenyl, phenoxy, halophenoxy, and C₁-C₆hydroxyalkyl; (b) Het is a 5 or 6 membered, saturated or unsaturated,heterocyclic ring, containing one or more heteroatoms independentlyselected from nitrogen, sulfur, or oxygen, and where Ar₁ and Ar₂ are notortho to each other (but may be meta or para, such as, for a fivemembered ring they are 1,3, and for a 6 membered ring they are either1,3 or 1,4 respectively), and where said heterocyclic ring may also besubstituted with one or more substituents independently selected from H,F, Cl, Br, I, CN, NO₂, oxo, C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl,C₁-C₆ alkoxy, C₁-C₆ haloalkyl, C₁-C₆ haloalkoxy, S(═O)_(n)C₁-C₆ alkyl(where n=0-2), S(═O)_(n)C₁-C₆ haloalkyl (where n=0-2), OSO₂C₁-C₆haloalkyl, C(═O)OC₁-C₆ alkyl, C(═O)C₁-C₆ alkyl, C(═O)C₁-C₆ haloalkyl,phenyl, phenoxy, halophenoxy, and C₁-C₆ hydroxyalkyl; (c) Ar₂ isfuranyl, phenyl, pyridazinyl, pyridyl, pyrimidinyl, thienyl, substitutedfuranyl, substituted phenyl, substituted pyridazinyl, substitutedpyridyl, substituted pyrimidinyl, or substituted thienyl, wherein saidsubstituted furanyl, substituted phenyl, substituted pyridazinyl,substituted pyridyl, substituted pyrimidinyl, and substituted thienyl,have one or more substituents independently selected from H, F, Cl, Br,I, CN, NO₂, oxo, C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₁-C₆alkoxy, C₁-C₆ haloalkyl, C₁-C₆ haloalkoxy, S(═O)_(n)C₁-C₆ alkyl (wheren=0-2), S(═O)_(n)C₁-C₆ haloalkyl (where n=0-2), OSO₂C₁-C₆ haloalkyl,C(═O)OC₁-C₆ alkyl, C(═O)C₁-C₆ alkyl, C(═O)C₁-C₆ haloalkyl, phenyl,phenoxy, halophenoxy, and C₁-C₆ hydroxyalkyl; (d) J is O, N, NR5, CR5,or C═O; (e) L is a single or double bond; (f) K is CR5, C═O, N, NR5, orC═S; (g) Q is O or S; (h) R1 is C₁-C₆ alkyl, C₁-C₆ alkyl-O—C₁-C₆ alkyl,C₁-C₆ haloalkyl, halo, oxo, C₁-C₆ haloalkoxy, C₁-C₆ alkyl-O—C₁-C₆alkoxy, H, OH, C₁-C₆ alkoxy, C₂-C₆ alkenyloxy; (i) R2 is C₁-C₆ alkyl,C₁-C₆ alkyl-O—C₁-C₆ alkyl, C₁-C₆ haloalkyl, halo, oxo, C₁-C₆ haloalkoxy,C₁-C₆ alkyl-O—C₁-C₆ alkoxy, H, OH, C₁-C₆ alkoxy, C₂-C₆ alkenyloxy; (j)R3 is C₁-C₆ alkyl, C₁-C₆ alkyl-O—C₁-C₆ alkyl, C₁-C₆ haloalkyl, halo,oxo, C₁-C₆ haloalkoxy, C₁-C₆ alkyl-O—C₁-C₆ alkoxy, H, OH, C₁-C₆ alkoxy,C₂-C₆ alkenyloxy; (k) R4 is C₁-C₆ alkyl, C₁-C₆ alkyl-O—C₁-C₆ alkyl,C₁-C₆ haloalkyl, H, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₆ alkenyloxy;and (l) R5 is H or C₁-C₆ alkyl.
 19. A compound according to claim 18wherein: (a) Ar₁ is phenyl, pyridyl, thienyl, substituted phenyl,substituted pyridazinyl, or substituted pyridyl, wherein saidsubstituted phenyl has one or more substituents independently selectedfrom F, Cl, Br, I, CN, CH₃, C₃H₇, C₄H₉, OCH₃, OC₄H₉, CF₃, C₂F₅, C₃F₇,OCF₃, OC₂F₅, OCH₂CF₃, OCF₂CHF₂, SCF₃, SCH₃, S(═O)CF₃, S(═O)₂CF₃, OPhCl,and C(OH)C₂H₅, wherein said substituted pyridazinyl has one or more Cl,wherein said substituted pyridyl has one or more substituentsindependently selected from F, Cl, I, CF₃, OCF₃, OCF₂CHFCF₃, andOCH₂CF₃; (b) Het is imidazolyl, isoxazolyl, 1,3,4 oxadiazolyl,pyrazinyl, pyrazolinyl, pyrazolyl, pyridyl, pyrimidinyl, pyrrolyl,1,2,3,4-tetrazolyl, thiazolyl, 1,3,5-triazinyl, 1,2,3-triazolyl,1,2,4-triazolyl, substituted pyrazolinyl, substituted pyrimidinyl, orsubstituted 1,2,4-triazolyl, wherein said substituted pyrazolyl has oneor more substituents independently selected from H, CH₃, C₃H₇,C(═O)OCH₃, C(═O)OC₂H₅, and C(═O)OC₄H₉, wherein said substitutedpyrimidinyl has one or more substituents independently selected from CF₃and C₃F₇, wherein said substituted 1,2,4-triazolyl has one or moresubstituents selected from CH₃ and oxo; (c) Ar₂ is phenyl, thienyl, orsubstituted phenyl, wherein said substituted phenyl has one or moresubstituents independently selected from F, Cl, OCH₃, and CF₃; (d) J isNH, CH, CCH₃, or C═O; (e) L is a single or double bond; (f) K is C═O, N,NH, or C═S; (g) Q is O, or S; (h) R1 is OCH₃ or OC₂H₅; (i) R2 isOCH₂CH═CH₂, OCH₃, OC₂H₅, OC₃H₇, or OC₄H₉; (j) R3 is OH, OCH₃, OC₂H₅, orOC₃H₇; and (k) R4 is CH₃ or CH₂OCH₃.
 20. A process comprising applying acompound of claim 18 to a locus to control pests.